Canonical Allele Identifier: CA2499306844
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753335_140753337dup , CM000669.2:g.140753335_140753337dup GRCh38
NC_000007.13:g.140453135_140453137dup , CM000669.1:g.140453135_140453137dup GRCh37
NC_000007.12:g.140099604_140099606dup NCBI36
NG_007873.3:g.176428_176430dup , LRG_299:g.176428_176430dup

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1798_1800dup MANE Select ENSP00000493543.1:p.Val600_Lys601insVal
ENST00000288602.11:c.1918_1920dup ENSP00000288602.7:p.Val640_Lys641insVal
ENST00000479537.6:c.468_470dup
ENST00000496384.7:c.1798_1800dup ENSP00000419060.2:p.Val600_Lys601insVal
ENST00000497784.2:c.*1248_*1250dup ENSP00000420119.2:n.*1248_*1250dup
ENST00000642228.1:c.*876_*878dup ENSP00000493678.1:n.*876_*878dup
ENST00000642875.1:n.1259-3919_1259-3917dup
ENST00000644120.1:n.2188_2190dup
ENST00000644650.1:c.894_896dup
ENST00000644905.1:n.2680_2682dup
ENST00000644969.2:c.1918_1920dup MANE Plus Clinical ENSP00000496776.1:p.Val640_Lys641insVal
ENST00000646730.1:c.*374_*376dup ENSP00000494784.1:n.*374_*376dup
ENST00000646891.1:c.1798_1800dup ENSP00000493543.1:p.Val600_Lys601insVal
ENST00000647434.1:c.738-3919_738-3917dup ENSP00000495132.1:n.738-3919_738-3917dup
ENST00000288602.10:c.1798_1800dup ENSP00000288602.6:p.Val600_Lys601insVal
ENST00000479537.5:c.82_84dup ENSP00000418033.1:p.Val28_Lys29insVal
ENST00000496384.6:c.621_623dup
ENST00000497784.1:c.1833_1835dup ENSP00000420119.1:n.1833_1835dup
NM_004333.4:c.1798_1800dup , LRG_299t1:c.1798_1800dup NP_004324.2:p.Val600_Lys601insVal
XM_005250045.1:c.1798_1800dup XP_005250102.1:p.Val600_Lys601insVal
XM_005250046.1:c.1798_1800dup XP_005250103.1:p.Val600_Lys601insVal
XM_011516529.1:c.1798_1800dup XP_011514831.1:p.Val600_Lys601insVal
XM_011516530.1:c.1695-3919_1695-3917dup XP_011514832.1:n.1695-3919_1695-3917dup
XR_242190.1:n.1806_1808dup
XR_927520.1:n.1806_1808dup
XR_927521.1:n.1806_1808dup
XR_927522.1:n.1703-3919_1703-3917dup
XR_927523.1:n.1703-3919_1703-3917dup
NM_001354609.1:c.1798_1800dup NP_001341538.1:p.Val600_Lys601insVal
NM_004333.5:c.1798_1800dup NP_004324.2:p.Val600_Lys601insVal
NR_148928.1:n.2896_2898dup
XM_017012558.1:c.1918_1920dup XP_016868047.1:p.Val640_Lys641insVal
XM_017012559.1:c.1918_1920dup XP_016868048.1:p.Val640_Lys641insVal
XR_001744857.1:n.1926_1928dup
XR_001744858.1:n.1823-3919_1823-3917dup
NM_001354609.2:c.1798_1800dup NP_001341538.1:p.Val600_Lys601insVal
NM_001374244.1:c.1918_1920dup NP_001361173.1:p.Val640_Lys641insVal
NM_001374258.1:c.1918_1920dup MANE Plus Clinical NP_001361187.1:p.Val640_Lys641insVal
NM_004333.6:c.1798_1800dup MANE Select NP_004324.2:p.Val600_Lys601insVal
NM_001378467.1:c.1807_1809dup NP_001365396.1:p.Val603_Lys604insVal
NM_001378468.1:c.1798_1800dup NP_001365397.1:p.Val600_Lys601insVal
NM_001378469.1:c.1732_1734dup NP_001365398.1:p.Val578_Lys579insVal
NM_001378470.1:c.1696_1698dup NP_001365399.1:p.Val566_Lys567insVal
NM_001378471.1:c.1687_1689dup NP_001365400.1:p.Val563_Lys564insVal
NM_001378472.1:c.1642_1644dup NP_001365401.1:p.Val548_Lys549insVal
NM_001378473.1:c.1642_1644dup NP_001365402.1:p.Val548_Lys549insVal
NM_001378474.1:c.1798_1800dup NP_001365403.1:p.Val600_Lys601insVal
NM_001378475.1:c.1534_1536dup NP_001365404.1:p.Val512_Lys513insVal