Canonical Allele Identifier: CA891842051
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753350_140753351insTCGAGATTCACTGTAGCTAGACCA , CM000669.2:g.140753350_140753351insTCGAGATTCACTGTAGCTAGACCA GRCh38
NC_000007.13:g.140453150_140453151insTCGAGATTCACTGTAGCTAGACCA , CM000669.1:g.140453150_140453151insTCGAGATTCACTGTAGCTAGACCA GRCh37
NC_000007.12:g.140099619_140099620insTCGAGATTCACTGTAGCTAGACCA NCBI36
NG_007873.3:g.176432_176433insTCTCGATGGTCTAGCTACAGTGAA , LRG_299:g.176432_176433insTCTCGATGGTCTAGCTACAGTGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA MANE Select ENSP00000493543.1:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
ENST00000288602.11:c.1922_1923insTCTCGATGGTCTAGCTACAGTGAA ENSP00000288602.7:p.Val640_Lys641insAsnLeuAspGlyLeuAlaThrVal
ENST00000479537.6:c.472_473insTCTCGATGGTCTAGCTACAGTGAA
ENST00000496384.7:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA ENSP00000419060.2:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
ENST00000497784.2:c.*1252_*1253insTCTCGATGGTCTAGCTACAGTGAA ENSP00000420119.2:n.*1252_*1253insTCTCGATGGTCTAGCTACAGTGAA
ENST00000642228.1:c.*880_*881insTCTCGATGGTCTAGCTACAGTGAA ENSP00000493678.1:n.*880_*881insTCTCGATGGTCTAGCTACAGTGAA
ENST00000642875.1:n.1259-3915_1259-3914insTCTCGATGGTCTAGCTACAGTGAA
ENST00000644120.1:n.2192_2193insTCTCGATGGTCTAGCTACAGTGAA
ENST00000644650.1:c.898_899insTCTCGATGGTCTAGCTACAGTGAA
ENST00000644905.1:n.2684_2685insTCTCGATGGTCTAGCTACAGTGAA
ENST00000644969.2:c.1922_1923insTCTCGATGGTCTAGCTACAGTGAA MANE Plus Clinical ENSP00000496776.1:p.Val640_Lys641insAsnLeuAspGlyLeuAlaThrVal
ENST00000646730.1:c.*378_*379insTCTCGATGGTCTAGCTACAGTGAA ENSP00000494784.1:n.*378_*379insTCTCGATGGTCTAGCTACAGTGAA
ENST00000646891.1:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA ENSP00000493543.1:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
ENST00000647434.1:c.738-3915_738-3914insTCTCGATGGTCTAGCTACAGTGAA ENSP00000495132.1:n.738-3915_738-3914insTCTCGATGGTCTAGCTACAGT...
ENST00000288602.10:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA ENSP00000288602.6:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
ENST00000479537.5:c.86_87insTCTCGATGGTCTAGCTACAGTGAA ENSP00000418033.1:p.Val28_Lys29insAsnLeuAspGlyLeuAlaThrVal
ENST00000496384.6:c.625_626insTCTCGATGGTCTAGCTACAGTGAA
ENST00000497784.1:c.1837_1838insTCTCGATGGTCTAGCTACAGTGAA ENSP00000420119.1:n.1837_1838insTCTCGATGGTCTAGCTACAGTGAA
NM_004333.4:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA , LRG_299t1:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA NP_004324.2:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
XM_005250045.1:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA XP_005250102.1:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
XM_005250046.1:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA XP_005250103.1:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
XM_011516529.1:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA XP_011514831.1:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
XM_011516530.1:c.1695-3915_1695-3914insTCTCGATGGTCTAGCTACAGTGAA XP_011514832.1:n.1695-3915_1695-3914insTCTCGATGGTCTAGCTACAGTG...
XR_242190.1:n.1810_1811insTCTCGATGGTCTAGCTACAGTGAA
XR_927520.1:n.1810_1811insTCTCGATGGTCTAGCTACAGTGAA
XR_927521.1:n.1810_1811insTCTCGATGGTCTAGCTACAGTGAA
XR_927522.1:n.1703-3915_1703-3914insTCTCGATGGTCTAGCTACAGTGAA
XR_927523.1:n.1703-3915_1703-3914insTCTCGATGGTCTAGCTACAGTGAA
NM_001354609.1:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA NP_001341538.1:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
NM_004333.5:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA NP_004324.2:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
NR_148928.1:n.2900_2901insTCTCGATGGTCTAGCTACAGTGAA
XM_017012558.1:c.1922_1923insTCTCGATGGTCTAGCTACAGTGAA XP_016868047.1:p.Val640_Lys641insAsnLeuAspGlyLeuAlaThrVal
XM_017012559.1:c.1922_1923insTCTCGATGGTCTAGCTACAGTGAA XP_016868048.1:p.Val640_Lys641insAsnLeuAspGlyLeuAlaThrVal
XR_001744857.1:n.1930_1931insTCTCGATGGTCTAGCTACAGTGAA
XR_001744858.1:n.1823-3915_1823-3914insTCTCGATGGTCTAGCTACAGTGAA
NM_001354609.2:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA NP_001341538.1:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
NM_001374244.1:c.1922_1923insTCTCGATGGTCTAGCTACAGTGAA NP_001361173.1:p.Val640_Lys641insAsnLeuAspGlyLeuAlaThrVal
NM_001374258.1:c.1922_1923insTCTCGATGGTCTAGCTACAGTGAA MANE Plus Clinical NP_001361187.1:p.Val640_Lys641insAsnLeuAspGlyLeuAlaThrVal
NM_004333.6:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA MANE Select NP_004324.2:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
NM_001378467.1:c.1811_1812insTCTCGATGGTCTAGCTACAGTGAA NP_001365396.1:p.Val603_Lys604insAsnLeuAspGlyLeuAlaThrVal
NM_001378468.1:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA NP_001365397.1:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
NM_001378469.1:c.1736_1737insTCTCGATGGTCTAGCTACAGTGAA NP_001365398.1:p.Val578_Lys579insAsnLeuAspGlyLeuAlaThrVal
NM_001378470.1:c.1700_1701insTCTCGATGGTCTAGCTACAGTGAA NP_001365399.1:p.Val566_Lys567insAsnLeuAspGlyLeuAlaThrVal
NM_001378471.1:c.1691_1692insTCTCGATGGTCTAGCTACAGTGAA NP_001365400.1:p.Val563_Lys564insAsnLeuAspGlyLeuAlaThrVal
NM_001378472.1:c.1646_1647insTCTCGATGGTCTAGCTACAGTGAA NP_001365401.1:p.Val548_Lys549insAsnLeuAspGlyLeuAlaThrVal
NM_001378473.1:c.1646_1647insTCTCGATGGTCTAGCTACAGTGAA NP_001365402.1:p.Val548_Lys549insAsnLeuAspGlyLeuAlaThrVal
NM_001378474.1:c.1802_1803insTCTCGATGGTCTAGCTACAGTGAA NP_001365403.1:p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal
NM_001378475.1:c.1538_1539insTCTCGATGGTCTAGCTACAGTGAA NP_001365404.1:p.Val512_Lys513insAsnLeuAspGlyLeuAlaThrVal