Canonical Allele Identifier: CA458115939
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs761120820
MyVariant Identifiers: chr7:g.140481416T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781616T>G , CM000669.2:g.140781616T>G GRCh38
NC_000007.13:g.140481416T>G , CM000669.1:g.140481416T>G GRCh37
NC_000007.12:g.140127885T>G NCBI36
NG_007873.3:g.148149A>C , LRG_299:g.148149A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1392A>C MANE Select ENSP00000493543.1:p.Gly464=
ENST00000288602.11:c.1512A>C ENSP00000288602.7:p.Gly504=
ENST00000479537.6:c.62A>C
ENST00000496384.7:c.1392A>C ENSP00000419060.2:p.Gly464=
ENST00000497784.2:c.*842A>C ENSP00000420119.2:n.*842A>C
ENST00000642228.1:c.*470A>C ENSP00000493678.1:n.*470A>C
ENST00000642875.1:n.834A>C
ENST00000644120.1:n.1782A>C
ENST00000644650.1:c.488A>C
ENST00000644905.1:n.1481A>C
ENST00000644969.2:c.1512A>C MANE Plus Clinical ENSP00000496776.1:p.Gly504=
ENST00000646334.1:n.522A>C
ENST00000646730.1:c.1392A>C ENSP00000494784.1:p.Gly464=
ENST00000646891.1:c.1392A>C ENSP00000493543.1:p.Gly464=
ENST00000647434.1:c.435A>C ENSP00000495132.1:p.Gly145=
ENST00000288602.10:c.1392A>C ENSP00000288602.6:p.Gly464=
ENST00000496384.6:c.215A>C
ENST00000497784.1:c.1427A>C ENSP00000420119.1:n.1427A>C
NM_004333.4:c.1392A>C , LRG_299t1:c.1392A>C NP_004324.2:p.Gly464=
XM_005250045.1:c.1392A>C XP_005250102.1:p.Gly464=
XM_005250046.1:c.1392A>C XP_005250103.1:p.Gly464=
XM_011516529.1:c.1392A>C XP_011514831.1:p.Gly464=
XM_011516530.1:c.1392A>C XP_011514832.1:p.Gly464=
XR_242190.1:n.1400A>C
XR_927520.1:n.1400A>C
XR_927521.1:n.1400A>C
XR_927522.1:n.1400A>C
XR_927523.1:n.1400A>C
NM_001354609.1:c.1392A>C NP_001341538.1:p.Gly464=
NM_004333.5:c.1392A>C NP_004324.2:p.Gly464=
NR_148928.1:n.1697A>C
XM_017012558.1:c.1512A>C XP_016868047.1:p.Gly504=
XM_017012559.1:c.1512A>C XP_016868048.1:p.Gly504=
XR_001744857.1:n.1520A>C
XR_001744858.1:n.1520A>C
NM_001354609.2:c.1392A>C NP_001341538.1:p.Gly464=
NM_001374244.1:c.1512A>C NP_001361173.1:p.Gly504=
NM_001374258.1:c.1512A>C MANE Plus Clinical NP_001361187.1:p.Gly504=
NM_004333.6:c.1392A>C MANE Select NP_004324.2:p.Gly464=
NM_001378467.1:c.1401A>C NP_001365396.1:p.Gly467=
NM_001378468.1:c.1392A>C NP_001365397.1:p.Gly464=
NM_001378469.1:c.1326A>C NP_001365398.1:p.Gly442=
NM_001378470.1:c.1290A>C NP_001365399.1:p.Gly430=
NM_001378471.1:c.1281A>C NP_001365400.1:p.Gly427=
NM_001378472.1:c.1236A>C NP_001365401.1:p.Gly412=
NM_001378473.1:c.1236A>C NP_001365402.1:p.Gly412=
NM_001378474.1:c.1392A>C NP_001365403.1:p.Gly464=
NM_001378475.1:c.1128A>C NP_001365404.1:p.Gly376=