Canonical Allele Identifier: CA1747709964
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753244_140753245delinsTA , CM000669.2:g.140753244_140753245delinsTA GRCh38
NC_000007.13:g.140453044_140453045delinsTA , CM000669.1:g.140453044_140453045delinsTA GRCh37
NC_000007.12:g.140099513_140099514delinsTA NCBI36
NG_007873.3:g.176520_176521delinsTA , LRG_299:g.176520_176521delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1860+30_1860+31delinsTA MANE Select ENSP00000493543.1:n.1860+30_1860+31delins...
ENST00000288602.11:c.1980+30_1980+31delinsTA ENSP00000288602.7:n.1980+30_1980+31delins...
ENST00000479537.6:c.530+30_530+31delinsTA
ENST00000496384.7:c.1860+30_1860+31delinsTA ENSP00000419060.2:n.1860+30_1860+31delins...
ENST00000497784.2:c.*1310+30_*1310+31delinsTA ENSP00000420119.2:n.*1310+30_*1310+31deli...
ENST00000642228.1:c.*938+30_*938+31delinsTA ENSP00000493678.1:n.*938+30_*938+31delins...
ENST00000642875.1:n.1259-3827_1259-3826delinsTA
ENST00000644120.1:n.2250+30_2250+31delinsTA
ENST00000644650.1:c.956+30_956+31delinsTA
ENST00000644905.1:n.2742+30_2742+31delinsTA
ENST00000644969.2:c.1980+30_1980+31delinsTA MANE Plus Clinical ENSP00000496776.1:n.1980+30_1980+31delins...
ENST00000646730.1:c.*436+30_*436+31delinsTA ENSP00000494784.1:n.*436+30_*436+31delins...
ENST00000646891.1:c.1860+30_1860+31delinsTA ENSP00000493543.1:n.1860+30_1860+31delins...
ENST00000647434.1:c.738-3827_738-3826delinsTA ENSP00000495132.1:n.738-3827_738-3826deli...
ENST00000288602.10:c.1860+30_1860+31delinsTA ENSP00000288602.6:n.1860+30_1860+31delins...
ENST00000479537.5:c.144+30_144+31delinsTA ENSP00000418033.1:n.144+30_144+31delinsTA...
ENST00000496384.6:c.683+30_683+31delinsTA
ENST00000497784.1:c.1895+30_1895+31delinsTA ENSP00000420119.1:n.1895+30_1895+31delins...
NM_004333.4:c.1860+30_1860+31delinsTA , LRG_299t1:c.1860+30_1860+31delinsTA NP_004324.2:n.1860+30_1860+31delinsTA
XM_005250045.1:c.1860+30_1860+31delinsTA XP_005250102.1:n.1860+30_1860+31delinsTA
XM_005250046.1:c.1860+30_1860+31delinsTA XP_005250103.1:n.1860+30_1860+31delinsTA
XM_011516529.1:c.1860+30_1860+31delinsTA XP_011514831.1:n.1860+30_1860+31delinsTA
XM_011516530.1:c.1695-3827_1695-3826delinsTA XP_011514832.1:n.1695-3827_1695-3826delin...
XR_242190.1:n.1868+30_1868+31delinsTA
XR_927520.1:n.1868+30_1868+31delinsTA
XR_927521.1:n.1868+30_1868+31delinsTA
XR_927522.1:n.1703-3827_1703-3826delinsTA
XR_927523.1:n.1703-3827_1703-3826delinsTA
NM_001354609.1:c.1860+30_1860+31delinsTA NP_001341538.1:n.1860+30_1860+31delinsTA
NM_004333.5:c.1860+30_1860+31delinsTA NP_004324.2:n.1860+30_1860+31delinsTA
NR_148928.1:n.2958+30_2958+31delinsTA
XM_017012558.1:c.1980+30_1980+31delinsTA XP_016868047.1:n.1980+30_1980+31delinsTA
XM_017012559.1:c.1980+30_1980+31delinsTA XP_016868048.1:n.1980+30_1980+31delinsTA
XR_001744857.1:n.1988+30_1988+31delinsTA
XR_001744858.1:n.1823-3827_1823-3826delinsTA
NM_001354609.2:c.1860+30_1860+31delinsTA NP_001341538.1:n.1860+30_1860+31delinsTA
NM_001374244.1:c.1980+30_1980+31delinsTA NP_001361173.1:n.1980+30_1980+31delinsTA
NM_001374258.1:c.1980+30_1980+31delinsTA MANE Plus Clinical NP_001361187.1:n.1980+30_1980+31delinsTA
NM_004333.6:c.1860+30_1860+31delinsTA MANE Select NP_004324.2:n.1860+30_1860+31delinsTA
NM_001378467.1:c.1869+30_1869+31delinsTA NP_001365396.1:n.1869+30_1869+31delinsTA
NM_001378468.1:c.1860+30_1860+31delinsTA NP_001365397.1:n.1860+30_1860+31delinsTA
NM_001378469.1:c.1794+30_1794+31delinsTA NP_001365398.1:n.1794+30_1794+31delinsTA
NM_001378470.1:c.1758+30_1758+31delinsTA NP_001365399.1:n.1758+30_1758+31delinsTA
NM_001378471.1:c.1749+30_1749+31delinsTA NP_001365400.1:n.1749+30_1749+31delinsTA
NM_001378472.1:c.1704+30_1704+31delinsTA NP_001365401.1:n.1704+30_1704+31delinsTA
NM_001378473.1:c.1704+30_1704+31delinsTA NP_001365402.1:n.1704+30_1704+31delinsTA
NM_001378474.1:c.1860+30_1860+31delinsTA NP_001365403.1:n.1860+30_1860+31delinsTA
NM_001378475.1:c.1596+30_1596+31delinsTA NP_001365404.1:n.1596+30_1596+31delinsTA