Canonical Allele Identifier: CA369588403

Gene: BRAF

Linked Data

• dbSNP Id: rs1370423184
• COSMIC: COSM4665999
• MyVariant Identifiers: chr7:g.140477818G>A (hg19) ; chr7:g.140778018G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140778018G>A , CM000669.2:g.140778018G>A	GRCh38
NC_000007.13:g.140477818G>A , CM000669.1:g.140477818G>A	GRCh37
NC_000007.12:g.140124287G>A	NCBI36
NG_007873.3:g.151747C>T , LRG_299:g.151747C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1490C>T MANE Select	ENSP00000493543.1:p.Ala497Val
ENST00000288602.11:c.1610C>T	ENSP00000288602.7:p.Ala537Val
ENST00000479537.6:c.160C>T
ENST00000496384.7:c.1490C>T	ENSP00000419060.2:p.Ala497Val
ENST00000497784.2:c.*940C>T	ENSP00000420119.2:n.*940C>T
ENST00000642228.1:c.*568C>T	ENSP00000493678.1:n.*568C>T
ENST00000642875.1:n.1054C>T
ENST00000644120.1:n.1880C>T
ENST00000644650.1:c.586C>T
ENST00000644905.1:n.1579C>T
ENST00000644969.2:c.1610C>T MANE Plus Clinical	ENSP00000496776.1:p.Ala537Val
ENST00000646730.1:c.1490C>T	ENSP00000494784.1:p.Ala497Val
ENST00000646891.1:c.1490C>T	ENSP00000493543.1:p.Ala497Val
ENST00000647434.1:c.533C>T	ENSP00000495132.1:p.Ala178Val
ENST00000288602.10:c.1490C>T	ENSP00000288602.6:p.Ala497Val
ENST00000496384.6:c.313C>T
ENST00000497784.1:c.1525C>T	ENSP00000420119.1:n.1525C>T
NM_004333.4:c.1490C>T , LRG_299t1:c.1490C>T	NP_004324.2:p.Ala497Val
XM_005250045.1:c.1490C>T	XP_005250102.1:p.Ala497Val
XM_005250046.1:c.1490C>T	XP_005250103.1:p.Ala497Val
XM_011516529.1:c.1490C>T	XP_011514831.1:p.Ala497Val
XM_011516530.1:c.1490C>T	XP_011514832.1:p.Ala497Val
XR_242190.1:n.1498C>T
XR_927520.1:n.1498C>T
XR_927521.1:n.1498C>T
XR_927522.1:n.1498C>T
XR_927523.1:n.1498C>T
NM_001354609.1:c.1490C>T	NP_001341538.1:p.Ala497Val
NM_004333.5:c.1490C>T	NP_004324.2:p.Ala497Val
NR_148928.1:n.1795C>T
XM_017012558.1:c.1610C>T	XP_016868047.1:p.Ala537Val
XM_017012559.1:c.1610C>T	XP_016868048.1:p.Ala537Val
XR_001744857.1:n.1618C>T
XR_001744858.1:n.1618C>T
NM_001354609.2:c.1490C>T	NP_001341538.1:p.Ala497Val
NM_001374244.1:c.1610C>T	NP_001361173.1:p.Ala537Val
NM_001374258.1:c.1610C>T MANE Plus Clinical	NP_001361187.1:p.Ala537Val
NM_004333.6:c.1490C>T MANE Select	NP_004324.2:p.Ala497Val
NM_001378467.1:c.1499C>T	NP_001365396.1:p.Ala500Val
NM_001378468.1:c.1490C>T	NP_001365397.1:p.Ala497Val
NM_001378469.1:c.1424C>T	NP_001365398.1:p.Ala475Val
NM_001378470.1:c.1388C>T	NP_001365399.1:p.Ala463Val
NM_001378471.1:c.1379C>T	NP_001365400.1:p.Ala460Val
NM_001378472.1:c.1334C>T	NP_001365401.1:p.Ala445Val
NM_001378473.1:c.1334C>T	NP_001365402.1:p.Ala445Val
NM_001378474.1:c.1490C>T	NP_001365403.1:p.Ala497Val
NM_001378475.1:c.1226C>T	NP_001365404.1:p.Ala409Val