Canonical Allele Identifier: CA369538521

Gene: BRAF

Linked Data

• dbSNP Id: rs397507485
• MyVariant Identifiers: chr7:g.140439727C>G (hg19) ; chr7:g.140739927C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739927C>G , CM000669.2:g.140739927C>G	GRCh38
NC_000007.13:g.140439727C>G , CM000669.1:g.140439727C>G	GRCh37
NC_000007.12:g.140086196C>G	NCBI36
NG_007873.3:g.189838G>C , LRG_299:g.189838G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.2012G>C MANE Select	ENSP00000493543.1:p.Arg671Pro
ENST00000288602.11:c.2132G>C	ENSP00000288602.7:p.Arg711Pro
ENST00000479537.6:c.764G>C
ENST00000496384.7:c.2012G>C	ENSP00000419060.2:p.Arg671Pro
ENST00000497784.2:c.*1462G>C	ENSP00000420119.2:n.*1462G>C
ENST00000642228.1:c.*1090G>C	ENSP00000493678.1:n.*1090G>C
ENST00000642875.1:n.1410G>C
ENST00000644120.1:n.2402G>C
ENST00000644650.1:c.1311G>C
ENST00000644905.1:n.2894G>C
ENST00000644969.2:c.2132G>C MANE Plus Clinical	ENSP00000496776.1:p.Arg711Pro
ENST00000645443.1:n.1791G>C
ENST00000646730.1:c.*670G>C	ENSP00000494784.1:n.*670G>C
ENST00000646891.1:c.2012G>C	ENSP00000493543.1:p.Arg671Pro
ENST00000647434.1:c.889G>C	ENSP00000495132.1:n.889G>C
ENST00000288602.10:c.2012G>C	ENSP00000288602.6:p.Arg671Pro
ENST00000479537.5:c.378G>C	ENSP00000418033.1:n.378G>C
ENST00000496384.6:c.835G>C
ENST00000497784.1:c.2047G>C	ENSP00000420119.1:n.2047G>C
NM_004333.4:c.2012G>C , LRG_299t1:c.2012G>C	NP_004324.2:p.Arg671Pro
XM_005250045.1:c.2012G>C	XP_005250102.1:p.Arg671Pro
XM_005250046.1:c.2012G>C	XP_005250103.1:p.Arg671Pro
XM_011516529.1:c.2012G>C	XP_011514831.1:p.Arg671Pro
XR_242190.1:n.2102G>C
XR_927520.1:n.2141G>C
XR_927521.1:n.2223G>C
XR_927522.1:n.1854G>C
XR_927523.1:n.1936G>C
NM_001354609.1:c.2012G>C	NP_001341538.1:p.Arg671Pro
NM_004333.5:c.2012G>C	NP_004324.2:p.Arg671Pro
NR_148928.1:n.3110G>C
XM_017012558.1:c.2132G>C	XP_016868047.1:p.Arg711Pro
XM_017012559.1:c.2132G>C	XP_016868048.1:p.Arg711Pro
XR_001744857.1:n.2222G>C
XR_001744858.1:n.1974G>C
NM_001354609.2:c.2012G>C	NP_001341538.1:p.Arg671Pro
NM_001374244.1:c.2132G>C	NP_001361173.1:p.Arg711Pro
NM_001374258.1:c.2132G>C MANE Plus Clinical	NP_001361187.1:p.Arg711Pro
NM_004333.6:c.2012G>C MANE Select	NP_004324.2:p.Arg671Pro
NM_001378467.1:c.2021G>C	NP_001365396.1:p.Arg674Pro
NM_001378468.1:c.2012G>C	NP_001365397.1:p.Arg671Pro
NM_001378469.1:c.1946G>C	NP_001365398.1:p.Arg649Pro
NM_001378470.1:c.1910G>C	NP_001365399.1:p.Arg637Pro
NM_001378471.1:c.1901G>C	NP_001365400.1:p.Arg634Pro
NM_001378472.1:c.1856G>C	NP_001365401.1:p.Arg619Pro
NM_001378473.1:c.1856G>C	NP_001365402.1:p.Arg619Pro
NM_001378474.1:c.2012G>C	NP_001365403.1:p.Arg671Pro
NM_001378475.1:c.1748G>C	NP_001365404.1:p.Arg583Pro