Canonical Allele Identifier: CA369538503
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs1428696172

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140739924C>G , CM000669.2:g.140739924C>G GRCh38
NC_000007.13:g.140439724C>G , CM000669.1:g.140439724C>G GRCh37
NC_000007.12:g.140086193C>G NCBI36
NG_007873.3:g.189841G>C , LRG_299:g.189841G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.2015G>C MANE Select ENSP00000493543.1:p.Gly672Ala
ENST00000288602.11:c.2135G>C ENSP00000288602.7:p.Gly712Ala
ENST00000479537.6:c.767G>C
ENST00000496384.7:c.2015G>C ENSP00000419060.2:p.Gly672Ala
ENST00000497784.2:c.*1465G>C ENSP00000420119.2:n.*1465G>C
ENST00000642228.1:c.*1093G>C ENSP00000493678.1:n.*1093G>C
ENST00000642875.1:n.1413G>C
ENST00000644120.1:n.2405G>C
ENST00000644650.1:c.1314G>C
ENST00000644905.1:n.2897G>C
ENST00000644969.2:c.2135G>C MANE Plus Clinical ENSP00000496776.1:p.Gly712Ala
ENST00000645443.1:n.1794G>C
ENST00000646730.1:c.*673G>C ENSP00000494784.1:n.*673G>C
ENST00000646891.1:c.2015G>C ENSP00000493543.1:p.Gly672Ala
ENST00000647434.1:c.892G>C ENSP00000495132.1:n.892G>C
ENST00000288602.10:c.2015G>C ENSP00000288602.6:p.Gly672Ala
ENST00000479537.5:c.381G>C ENSP00000418033.1:n.381G>C
ENST00000496384.6:c.838G>C
ENST00000497784.1:c.2050G>C ENSP00000420119.1:n.2050G>C
NM_004333.4:c.2015G>C , LRG_299t1:c.2015G>C NP_004324.2:p.Gly672Ala
XM_005250045.1:c.2015G>C XP_005250102.1:p.Gly672Ala
XM_005250046.1:c.2015G>C XP_005250103.1:p.Gly672Ala
XM_011516529.1:c.2015G>C XP_011514831.1:p.Gly672Ala
XR_242190.1:n.2105G>C
XR_927520.1:n.2144G>C
XR_927521.1:n.2226G>C
XR_927522.1:n.1857G>C
XR_927523.1:n.1939G>C
NM_001354609.1:c.2015G>C NP_001341538.1:p.Gly672Ala
NM_004333.5:c.2015G>C NP_004324.2:p.Gly672Ala
NR_148928.1:n.3113G>C
XM_017012558.1:c.2135G>C XP_016868047.1:p.Gly712Ala
XM_017012559.1:c.2135G>C XP_016868048.1:p.Gly712Ala
XR_001744857.1:n.2225G>C
XR_001744858.1:n.1977G>C
NM_001354609.2:c.2015G>C NP_001341538.1:p.Gly672Ala
NM_001374244.1:c.2135G>C NP_001361173.1:p.Gly712Ala
NM_001374258.1:c.2135G>C MANE Plus Clinical NP_001361187.1:p.Gly712Ala
NM_004333.6:c.2015G>C MANE Select NP_004324.2:p.Gly672Ala
NM_001378467.1:c.2024G>C NP_001365396.1:p.Gly675Ala
NM_001378468.1:c.2015G>C NP_001365397.1:p.Gly672Ala
NM_001378469.1:c.1949G>C NP_001365398.1:p.Gly650Ala
NM_001378470.1:c.1913G>C NP_001365399.1:p.Gly638Ala
NM_001378471.1:c.1904G>C NP_001365400.1:p.Gly635Ala
NM_001378472.1:c.1859G>C NP_001365401.1:p.Gly620Ala
NM_001378473.1:c.1859G>C NP_001365402.1:p.Gly620Ala
NM_001378474.1:c.2015G>C NP_001365403.1:p.Gly672Ala
NM_001378475.1:c.1751G>C NP_001365404.1:p.Gly584Ala