Canonical Allele Identifier: CA369588171

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140476812A>G (hg19) ; chr7:g.140777012A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777012A>G , CM000669.2:g.140777012A>G	GRCh38
NC_000007.13:g.140476812A>G , CM000669.1:g.140476812A>G	GRCh37
NC_000007.12:g.140123281A>G	NCBI36
NG_007873.3:g.152753T>C , LRG_299:g.152753T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1594T>C MANE Select	ENSP00000493543.1:p.Cys532Arg
ENST00000288602.11:c.1714T>C	ENSP00000288602.7:p.Cys572Arg
ENST00000479537.6:c.264T>C
ENST00000496384.7:c.1594T>C	ENSP00000419060.2:p.Cys532Arg
ENST00000497784.2:c.*1044T>C	ENSP00000420119.2:n.*1044T>C
ENST00000642228.1:c.*672T>C	ENSP00000493678.1:n.*672T>C
ENST00000642875.1:n.1158T>C
ENST00000644120.1:n.1984T>C
ENST00000644650.1:c.690T>C
ENST00000644905.1:n.1683T>C
ENST00000644969.2:c.1714T>C MANE Plus Clinical	ENSP00000496776.1:p.Cys572Arg
ENST00000646730.1:c.1594T>C	ENSP00000494784.1:p.Cys532Arg
ENST00000646891.1:c.1594T>C	ENSP00000493543.1:p.Cys532Arg
ENST00000647434.1:c.637T>C	ENSP00000495132.1:p.Cys213Arg
ENST00000288602.10:c.1594T>C	ENSP00000288602.6:p.Cys532Arg
ENST00000496384.6:c.417T>C
ENST00000497784.1:c.1629T>C	ENSP00000420119.1:n.1629T>C
NM_004333.4:c.1594T>C , LRG_299t1:c.1594T>C	NP_004324.2:p.Cys532Arg
XM_005250045.1:c.1594T>C	XP_005250102.1:p.Cys532Arg
XM_005250046.1:c.1594T>C	XP_005250103.1:p.Cys532Arg
XM_011516529.1:c.1594T>C	XP_011514831.1:p.Cys532Arg
XM_011516530.1:c.1594T>C	XP_011514832.1:p.Cys532Arg
XR_242190.1:n.1602T>C
XR_927520.1:n.1602T>C
XR_927521.1:n.1602T>C
XR_927522.1:n.1602T>C
XR_927523.1:n.1602T>C
NM_001354609.1:c.1594T>C	NP_001341538.1:p.Cys532Arg
NM_004333.5:c.1594T>C	NP_004324.2:p.Cys532Arg
NR_148928.1:n.1899T>C
XM_017012558.1:c.1714T>C	XP_016868047.1:p.Cys572Arg
XM_017012559.1:c.1714T>C	XP_016868048.1:p.Cys572Arg
XR_001744857.1:n.1722T>C
XR_001744858.1:n.1722T>C
NM_001354609.2:c.1594T>C	NP_001341538.1:p.Cys532Arg
NM_001374244.1:c.1714T>C	NP_001361173.1:p.Cys572Arg
NM_001374258.1:c.1714T>C MANE Plus Clinical	NP_001361187.1:p.Cys572Arg
NM_004333.6:c.1594T>C MANE Select	NP_004324.2:p.Cys532Arg
NM_001378467.1:c.1603T>C	NP_001365396.1:p.Cys535Arg
NM_001378468.1:c.1594T>C	NP_001365397.1:p.Cys532Arg
NM_001378469.1:c.1528T>C	NP_001365398.1:p.Cys510Arg
NM_001378470.1:c.1492T>C	NP_001365399.1:p.Cys498Arg
NM_001378471.1:c.1483T>C	NP_001365400.1:p.Cys495Arg
NM_001378472.1:c.1438T>C	NP_001365401.1:p.Cys480Arg
NM_001378473.1:c.1438T>C	NP_001365402.1:p.Cys480Arg
NM_001378474.1:c.1594T>C	NP_001365403.1:p.Cys532Arg
NM_001378475.1:c.1330T>C	NP_001365404.1:p.Cys444Arg