Canonical Allele Identifier: CA279976
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13979
dbSNP Id: rs180177040

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140754187T>C , CM000669.2:g.140754187T>C GRCh38
NC_000007.13:g.140453987T>C , CM000669.1:g.140453987T>C GRCh37
NC_000007.12:g.140100456T>C NCBI36
NG_007873.3:g.175578A>G , LRG_299:g.175578A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1741A>G MANE Select ENSP00000493543.1:p.Asn581Asp
ENST00000288602.11:c.1861A>G ENSP00000288602.7:p.Asn621Asp
ENST00000479537.6:c.411A>G
ENST00000496384.7:c.1741A>G ENSP00000419060.2:p.Asn581Asp
ENST00000497784.2:c.*1191A>G ENSP00000420119.2:n.*1191A>G
ENST00000642228.1:c.*819A>G ENSP00000493678.1:n.*819A>G
ENST00000642875.1:n.1259-4769A>G
ENST00000644120.1:n.2131A>G
ENST00000644650.1:c.837A>G
ENST00000644905.1:n.1830A>G
ENST00000644969.2:c.1861A>G MANE Plus Clinical ENSP00000496776.1:p.Asn621Asp
ENST00000646730.1:c.*317A>G ENSP00000494784.1:n.*317A>G
ENST00000646891.1:c.1741A>G ENSP00000493543.1:p.Asn581Asp
ENST00000647434.1:c.738-4769A>G ENSP00000495132.1:n.738-4769A>G
ENST00000288602.10:c.1741A>G ENSP00000288602.6:p.Asn581Asp
ENST00000479537.5:c.25A>G ENSP00000418033.1:p.Asn9Asp
ENST00000496384.6:c.564A>G
ENST00000497784.1:c.1776A>G ENSP00000420119.1:n.1776A>G
NM_004333.4:c.1741A>G , LRG_299t1:c.1741A>G NP_004324.2:p.Asn581Asp
XM_005250045.1:c.1741A>G XP_005250102.1:p.Asn581Asp
XM_005250046.1:c.1741A>G XP_005250103.1:p.Asn581Asp
XM_011516529.1:c.1741A>G XP_011514831.1:p.Asn581Asp
XM_011516530.1:c.1695-4769A>G XP_011514832.1:n.1695-4769A>G
XR_242190.1:n.1749A>G
XR_927520.1:n.1749A>G
XR_927521.1:n.1749A>G
XR_927522.1:n.1703-4769A>G
XR_927523.1:n.1703-4769A>G
NM_001354609.1:c.1741A>G NP_001341538.1:p.Asn581Asp
NM_004333.5:c.1741A>G NP_004324.2:p.Asn581Asp
NR_148928.1:n.2046A>G
XM_017012558.1:c.1861A>G XP_016868047.1:p.Asn621Asp
XM_017012559.1:c.1861A>G XP_016868048.1:p.Asn621Asp
XR_001744857.1:n.1869A>G
XR_001744858.1:n.1823-4769A>G
NM_001354609.2:c.1741A>G NP_001341538.1:p.Asn581Asp
NM_001374244.1:c.1861A>G NP_001361173.1:p.Asn621Asp
NM_001374258.1:c.1861A>G MANE Plus Clinical NP_001361187.1:p.Asn621Asp
NM_004333.6:c.1741A>G MANE Select NP_004324.2:p.Asn581Asp
NM_001378467.1:c.1750A>G NP_001365396.1:p.Asn584Asp
NM_001378468.1:c.1741A>G NP_001365397.1:p.Asn581Asp
NM_001378469.1:c.1675A>G NP_001365398.1:p.Asn559Asp
NM_001378470.1:c.1639A>G NP_001365399.1:p.Asn547Asp
NM_001378471.1:c.1630A>G NP_001365400.1:p.Asn544Asp
NM_001378472.1:c.1585A>G NP_001365401.1:p.Asn529Asp
NM_001378473.1:c.1585A>G NP_001365402.1:p.Asn529Asp
NM_001378474.1:c.1741A>G NP_001365403.1:p.Asn581Asp
NM_001378475.1:c.1477A>G NP_001365404.1:p.Asn493Asp