Canonical Allele Identifier: CA645544085
Gene: BRAF HGNC NCBI

Linked Data

COSMIC: COSM1129

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753321_140753336delinsT , CM000669.2:g.140753321_140753336delinsT GRCh38
NC_000007.13:g.140453121_140453136delinsT , CM000669.1:g.140453121_140453136delinsT GRCh37
NC_000007.12:g.140099590_140099605delinsT NCBI36
NG_007873.3:g.176429_176444delinsA , LRG_299:g.176429_176444delinsA

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1799_1814delinsA MANE Select ENSP00000493543.1:p.Val600_Ser605delinsAsp
ENST00000288602.11:c.1919_1934delinsA ENSP00000288602.7:p.Val640_Ser645delinsAsp
ENST00000479537.6:c.469_484delinsA
ENST00000496384.7:c.1799_1814delinsA ENSP00000419060.2:p.Val600_Ser605delinsAsp
ENST00000497784.2:c.*1249_*1264delinsA ENSP00000420119.2:n.*1249_*1264delinsA
ENST00000642228.1:c.*877_*892delinsA ENSP00000493678.1:n.*877_*892delinsA
ENST00000642875.1:n.1259-3918_1259-3903delinsA
ENST00000644120.1:n.2189_2204delinsA
ENST00000644650.1:c.895_910delinsA
ENST00000644905.1:n.2681_2696delinsA
ENST00000644969.2:c.1919_1934delinsA MANE Plus Clinical ENSP00000496776.1:p.Val640_Ser645delinsAsp
ENST00000646730.1:c.*375_*390delinsA ENSP00000494784.1:n.*375_*390delinsA
ENST00000646891.1:c.1799_1814delinsA ENSP00000493543.1:p.Val600_Ser605delinsAsp
ENST00000647434.1:c.738-3918_738-3903delinsA ENSP00000495132.1:n.738-3918_738-3903delinsA
ENST00000288602.10:c.1799_1814delinsA ENSP00000288602.6:p.Val600_Ser605delinsAsp
ENST00000479537.5:c.83_98delinsA ENSP00000418033.1:p.Val28_Ser33delinsAsp
ENST00000496384.6:c.622_637delinsA
ENST00000497784.1:c.1834_1849delinsA ENSP00000420119.1:n.1834_1849delinsA
NM_004333.4:c.1799_1814delinsA , LRG_299t1:c.1799_1814delinsA NP_004324.2:p.Val600_Ser605delinsAsp
XM_005250045.1:c.1799_1814delinsA XP_005250102.1:p.Val600_Ser605delinsAsp
XM_005250046.1:c.1799_1814delinsA XP_005250103.1:p.Val600_Ser605delinsAsp
XM_011516529.1:c.1799_1814delinsA XP_011514831.1:p.Val600_Ser605delinsAsp
XM_011516530.1:c.1695-3918_1695-3903delinsA XP_011514832.1:n.1695-3918_1695-3903delinsA
XR_242190.1:n.1807_1822delinsA
XR_927520.1:n.1807_1822delinsA
XR_927521.1:n.1807_1822delinsA
XR_927522.1:n.1703-3918_1703-3903delinsA
XR_927523.1:n.1703-3918_1703-3903delinsA
NM_001354609.1:c.1799_1814delinsA NP_001341538.1:p.Val600_Ser605delinsAsp
NM_004333.5:c.1799_1814delinsA NP_004324.2:p.Val600_Ser605delinsAsp
NR_148928.1:n.2897_2912delinsA
XM_017012558.1:c.1919_1934delinsA XP_016868047.1:p.Val640_Ser645delinsAsp
XM_017012559.1:c.1919_1934delinsA XP_016868048.1:p.Val640_Ser645delinsAsp
XR_001744857.1:n.1927_1942delinsA
XR_001744858.1:n.1823-3918_1823-3903delinsA
NM_001354609.2:c.1799_1814delinsA NP_001341538.1:p.Val600_Ser605delinsAsp
NM_001374244.1:c.1919_1934delinsA NP_001361173.1:p.Val640_Ser645delinsAsp
NM_001374258.1:c.1919_1934delinsA MANE Plus Clinical NP_001361187.1:p.Val640_Ser645delinsAsp
NM_004333.6:c.1799_1814delinsA MANE Select NP_004324.2:p.Val600_Ser605delinsAsp
NM_001378467.1:c.1808_1823delinsA NP_001365396.1:p.Val603_Ser608delinsAsp
NM_001378468.1:c.1799_1814delinsA NP_001365397.1:p.Val600_Ser605delinsAsp
NM_001378469.1:c.1733_1748delinsA NP_001365398.1:p.Val578_Ser583delinsAsp
NM_001378470.1:c.1697_1712delinsA NP_001365399.1:p.Val566_Ser571delinsAsp
NM_001378471.1:c.1688_1703delinsA NP_001365400.1:p.Val563_Ser568delinsAsp
NM_001378472.1:c.1643_1658delinsA NP_001365401.1:p.Val548_Ser553delinsAsp
NM_001378473.1:c.1643_1658delinsA NP_001365402.1:p.Val548_Ser553delinsAsp
NM_001378474.1:c.1799_1814delinsA NP_001365403.1:p.Val600_Ser605delinsAsp
NM_001378475.1:c.1535_1550delinsA NP_001365404.1:p.Val512_Ser517delinsAsp