Canonical Allele Identifier: CA168047474
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs121913369
COSMIC: COSM133632

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NM_004333.4:c.1789C>T , LRG_299t1:c.1789C>T NP_004324.2:p.Leu597=
XM_005250045.1:c.1789C>T XP_005250102.1:p.Leu597=
XM_005250046.1:c.1789C>T XP_005250103.1:p.Leu597=
XM_011516529.1:c.1789C>T XP_011514831.1:p.Leu597=
XM_011516530.1:c.1695-3928C>T XP_011514832.1:p.=
XR_242190.1:n.1797C>T
XR_927520.1:n.1797C>T
XR_927521.1:n.1797C>T
XR_927522.1:n.1703-3928C>T
XR_927523.1:n.1703-3928C>T
NM_001354609.1:c.1789C>T NP_001341538.1:p.Leu597=
NM_004333.5:c.1789C>T NP_004324.2:p.Leu597=
NR_148928.1:n.2887C>T
XM_017012558.1:c.1909C>T XP_016868047.1:p.Leu637=
XM_017012559.1:c.1909C>T XP_016868048.1:p.Leu637=
XR_001744857.1:n.1917C>T
XR_001744858.1:n.1823-3928C>T
NM_001354609.2:c.1789C>T NP_001341538.1:p.Leu597=
NM_001374244.1:c.1909C>T NP_001361173.1:p.Leu637=
NM_001374258.1:c.1909C>T MANE Select NP_001361187.1:p.Leu637=
NM_004333.6:c.1789C>T NP_004324.2:p.Leu597=
NM_001378467.1:c.1798C>T NP_001365396.1:p.Leu600=
NM_001378468.1:c.1789C>T NP_001365397.1:p.Leu597=
NM_001378469.1:c.1723C>T NP_001365398.1:p.Leu575=
NM_001378470.1:c.1687C>T NP_001365399.1:p.Leu563=
NM_001378471.1:c.1678C>T NP_001365400.1:p.Leu560=
NM_001378472.1:c.1633C>T NP_001365401.1:p.Leu545=
NM_001378473.1:c.1633C>T NP_001365402.1:p.Leu545=
NM_001378474.1:c.1789C>T NP_001365403.1:p.Leu597=
NM_001378475.1:c.1525C>T NP_001365404.1:p.Leu509=
ENST00000288602.10:c.1789C>T ENSP00000288602.6:p.Leu597=
ENST00000479537.5:n.73C>T ENSP00000418033.1:p.Leu25=
ENST00000496384.6:n.612C>T
ENST00000497784.1:n.1824C>T ENSP00000420119.1:p.=