Canonical Allele Identifier: CA458116634

Gene: BRAF

Linked Data

• dbSNP Id: rs1255158411
• gnomAD v2: 7-140501223-A-G
• COSMIC: COSM6475271
• MyVariant Identifiers: chr7:g.140501223A>G (hg19) ; chr7:g.140801423A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801423A>G , CM000669.2:g.140801423A>G	GRCh38
NC_000007.13:g.140501223A>G , CM000669.1:g.140501223A>G	GRCh37
NC_000007.12:g.140147692A>G	NCBI36
NG_007873.3:g.128342T>C , LRG_299:g.128342T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.849T>C MANE Select	ENSP00000493543.1:p.Tyr283=
ENST00000288602.11:c.849T>C	ENSP00000288602.7:p.Tyr283=
ENST00000496384.7:c.849T>C	ENSP00000419060.2:p.Tyr283=
ENST00000497784.2:c.*299T>C	ENSP00000420119.2:n.*299T>C
ENST00000642228.1:c.849T>C	ENSP00000493678.1:p.Tyr283=
ENST00000642272.1:n.881T>C
ENST00000642875.1:n.343T>C
ENST00000643356.1:n.450T>C
ENST00000644120.1:n.1291T>C
ENST00000644905.1:n.938T>C
ENST00000644969.2:c.849T>C MANE Plus Clinical	ENSP00000496776.1:p.Tyr283=
ENST00000646730.1:c.849T>C	ENSP00000494784.1:p.Tyr283=
ENST00000646891.1:c.849T>C	ENSP00000493543.1:p.Tyr283=
ENST00000288602.10:c.849T>C	ENSP00000288602.6:p.Tyr283=
ENST00000497784.1:c.884T>C	ENSP00000420119.1:n.884T>C
NM_004333.4:c.849T>C , LRG_299t1:c.849T>C	NP_004324.2:p.Tyr283=
XM_005250045.1:c.849T>C	XP_005250102.1:p.Tyr283=
XM_005250046.1:c.849T>C	XP_005250103.1:p.Tyr283=
XM_011516529.1:c.849T>C	XP_011514831.1:p.Tyr283=
XM_011516530.1:c.849T>C	XP_011514832.1:p.Tyr283=
XR_242190.1:n.857T>C
XR_927520.1:n.857T>C
XR_927521.1:n.857T>C
XR_927522.1:n.857T>C
XR_927523.1:n.857T>C
NM_001354609.1:c.849T>C	NP_001341538.1:p.Tyr283=
NM_004333.5:c.849T>C	NP_004324.2:p.Tyr283=
NR_148928.1:n.1154T>C
XM_017012558.1:c.849T>C	XP_016868047.1:p.Tyr283=
XM_017012559.1:c.849T>C	XP_016868048.1:p.Tyr283=
XR_001744857.1:n.857T>C
XR_001744858.1:n.857T>C
NM_001354609.2:c.849T>C	NP_001341538.1:p.Tyr283=
NM_001374244.1:c.849T>C	NP_001361173.1:p.Tyr283=
NM_001374258.1:c.849T>C MANE Plus Clinical	NP_001361187.1:p.Tyr283=
NM_004333.6:c.849T>C MANE Select	NP_004324.2:p.Tyr283=
NM_001378467.1:c.858T>C	NP_001365396.1:p.Tyr286=
NM_001378468.1:c.849T>C	NP_001365397.1:p.Tyr283=
NM_001378469.1:c.849T>C	NP_001365398.1:p.Tyr283=
NM_001378470.1:c.747T>C	NP_001365399.1:p.Tyr249=
NM_001378471.1:c.849T>C	NP_001365400.1:p.Tyr283=
NM_001378472.1:c.693T>C	NP_001365401.1:p.Tyr231=
NM_001378473.1:c.693T>C	NP_001365402.1:p.Tyr231=
NM_001378474.1:c.849T>C	NP_001365403.1:p.Tyr283=
NM_001378475.1:c.585T>C	NP_001365404.1:p.Tyr195=