Canonical Allele Identifier: CA123651
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13969
dbSNP Id: rs121913369
COSMIC: COSM470
CIViC: CA123651

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753346G>C , CM000669.2:g.140753346G>C GRCh38
NC_000007.13:g.140453146G>C , CM000669.1:g.140453146G>C GRCh37
NC_000007.12:g.140099615G>C NCBI36
NG_007873.3:g.176419C>G , LRG_299:g.176419C>G

Transcript Alleles

HGVS Amino-acid change
NM_004333.4:c.1789C>G , LRG_299t1:c.1789C>G NP_004324.2:p.Leu597Val
XM_005250045.1:c.1789C>G XP_005250102.1:p.Leu597Val
XM_005250046.1:c.1789C>G XP_005250103.1:p.Leu597Val
XM_011516529.1:c.1789C>G XP_011514831.1:p.Leu597Val
XM_011516530.1:c.1695-3928C>G XP_011514832.1:p.=
XR_242190.1:n.1797C>G
XR_927520.1:n.1797C>G
XR_927521.1:n.1797C>G
XR_927522.1:n.1703-3928C>G
XR_927523.1:n.1703-3928C>G
NM_001354609.1:c.1789C>G NP_001341538.1:p.Leu597Val
NM_004333.5:c.1789C>G NP_004324.2:p.Leu597Val
NR_148928.1:n.2887C>G
XM_017012558.1:c.1909C>G XP_016868047.1:p.Leu637Val
XM_017012559.1:c.1909C>G XP_016868048.1:p.Leu637Val
XR_001744857.1:n.1917C>G
XR_001744858.1:n.1823-3928C>G
NM_001354609.2:c.1789C>G NP_001341538.1:p.Leu597Val
NM_001374244.1:c.1909C>G NP_001361173.1:p.Leu637Val
NM_001374258.1:c.1909C>G MANE Select NP_001361187.1:p.Leu637Val
NM_004333.6:c.1789C>G NP_004324.2:p.Leu597Val
NM_001378467.1:c.1798C>G NP_001365396.1:p.Leu600Val
NM_001378468.1:c.1789C>G NP_001365397.1:p.Leu597Val
NM_001378469.1:c.1723C>G NP_001365398.1:p.Leu575Val
NM_001378470.1:c.1687C>G NP_001365399.1:p.Leu563Val
NM_001378471.1:c.1678C>G NP_001365400.1:p.Leu560Val
NM_001378472.1:c.1633C>G NP_001365401.1:p.Leu545Val
NM_001378473.1:c.1633C>G NP_001365402.1:p.Leu545Val
NM_001378474.1:c.1789C>G NP_001365403.1:p.Leu597Val
NM_001378475.1:c.1525C>G NP_001365404.1:p.Leu509Val
ENST00000288602.10:c.1789C>G ENSP00000288602.6:p.Leu597Val
ENST00000479537.5:n.73C>G ENSP00000418033.1:p.Leu25Val
ENST00000496384.6:n.612C>G
ENST00000497784.1:n.1824C>G ENSP00000420119.1:p.=