Canonical Allele Identifier: CA2967272944
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753373_140753374insATATAT , CM000669.2:g.140753373_140753374insATATAT GRCh38
NC_000007.13:g.140453173_140453174insATATAT , CM000669.1:g.140453173_140453174insATATAT GRCh37
NC_000007.12:g.140099642_140099643insATATAT NCBI36
NG_007873.3:g.176391_176392insATATAT , LRG_299:g.176391_176392insATATAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1761_1762insATATAT MANE Select ENSP00000493543.1:p.Asp587_Leu588insIleTyr
ENST00000288602.11:c.1881_1882insATATAT ENSP00000288602.7:p.Asp627_Leu628insIleTyr
ENST00000479537.6:c.431_432insATATAT
ENST00000496384.7:c.1761_1762insATATAT ENSP00000419060.2:p.Asp587_Leu588insIleTyr
ENST00000497784.2:c.*1211_*1212insATATAT ENSP00000420119.2:n.*1211_*1212insATATAT
ENST00000642228.1:c.*839_*840insATATAT ENSP00000493678.1:n.*839_*840insATATAT
ENST00000642875.1:n.1259-3956_1259-3955insATATAT
ENST00000644120.1:n.2151_2152insATATAT
ENST00000644650.1:c.857_858insATATAT
ENST00000644905.1:n.2643_2644insATATAT
ENST00000644969.2:c.1881_1882insATATAT MANE Plus Clinical ENSP00000496776.1:p.Asp627_Leu628insIleTyr
ENST00000646730.1:c.*337_*338insATATAT ENSP00000494784.1:n.*337_*338insATATAT
ENST00000646891.1:c.1761_1762insATATAT ENSP00000493543.1:p.Asp587_Leu588insIleTyr
ENST00000647434.1:c.738-3956_738-3955insATATAT ENSP00000495132.1:n.738-3956_738-3955insATATAT
ENST00000288602.10:c.1761_1762insATATAT ENSP00000288602.6:p.Asp587_Leu588insIleTyr
ENST00000479537.5:c.45_46insATATAT ENSP00000418033.1:p.Asp15_Leu16insIleTyr
ENST00000496384.6:c.584_585insATATAT
ENST00000497784.1:c.1796_1797insATATAT ENSP00000420119.1:n.1796_1797insATATAT
NM_004333.4:c.1761_1762insATATAT , LRG_299t1:c.1761_1762insATATAT NP_004324.2:p.Asp587_Leu588insIleTyr
XM_005250045.1:c.1761_1762insATATAT XP_005250102.1:p.Asp587_Leu588insIleTyr
XM_005250046.1:c.1761_1762insATATAT XP_005250103.1:p.Asp587_Leu588insIleTyr
XM_011516529.1:c.1761_1762insATATAT XP_011514831.1:p.Asp587_Leu588insIleTyr
XM_011516530.1:c.1695-3956_1695-3955insATATAT XP_011514832.1:n.1695-3956_1695-3955insATATAT
XR_242190.1:n.1769_1770insATATAT
XR_927520.1:n.1769_1770insATATAT
XR_927521.1:n.1769_1770insATATAT
XR_927522.1:n.1703-3956_1703-3955insATATAT
XR_927523.1:n.1703-3956_1703-3955insATATAT
NM_001354609.1:c.1761_1762insATATAT NP_001341538.1:p.Asp587_Leu588insIleTyr
NM_004333.5:c.1761_1762insATATAT NP_004324.2:p.Asp587_Leu588insIleTyr
NR_148928.1:n.2859_2860insATATAT
XM_017012558.1:c.1881_1882insATATAT XP_016868047.1:p.Asp627_Leu628insIleTyr
XM_017012559.1:c.1881_1882insATATAT XP_016868048.1:p.Asp627_Leu628insIleTyr
XR_001744857.1:n.1889_1890insATATAT
XR_001744858.1:n.1823-3956_1823-3955insATATAT
NM_001354609.2:c.1761_1762insATATAT NP_001341538.1:p.Asp587_Leu588insIleTyr
NM_001374244.1:c.1881_1882insATATAT NP_001361173.1:p.Asp627_Leu628insIleTyr
NM_001374258.1:c.1881_1882insATATAT MANE Plus Clinical NP_001361187.1:p.Asp627_Leu628insIleTyr
NM_004333.6:c.1761_1762insATATAT MANE Select NP_004324.2:p.Asp587_Leu588insIleTyr
NM_001378467.1:c.1770_1771insATATAT NP_001365396.1:p.Asp590_Leu591insIleTyr
NM_001378468.1:c.1761_1762insATATAT NP_001365397.1:p.Asp587_Leu588insIleTyr
NM_001378469.1:c.1695_1696insATATAT NP_001365398.1:p.Asp565_Leu566insIleTyr
NM_001378470.1:c.1659_1660insATATAT NP_001365399.1:p.Asp553_Leu554insIleTyr
NM_001378471.1:c.1650_1651insATATAT NP_001365400.1:p.Asp550_Leu551insIleTyr
NM_001378472.1:c.1605_1606insATATAT NP_001365401.1:p.Asp535_Leu536insIleTyr
NM_001378473.1:c.1605_1606insATATAT NP_001365402.1:p.Asp535_Leu536insIleTyr
NM_001378474.1:c.1761_1762insATATAT NP_001365403.1:p.Asp587_Leu588insIleTyr
NM_001378475.1:c.1497_1498insATATAT NP_001365404.1:p.Asp499_Leu500insIleTyr