Canonical Allele Identifier: CA369588433

Gene: BRAF

Linked Data

• dbSNP Id: rs2129019585
• MyVariant Identifiers: chr7:g.140477829C>G (hg19) ; chr7:g.140778029C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140778029C>G , CM000669.2:g.140778029C>G	GRCh38
NC_000007.13:g.140477829C>G , CM000669.1:g.140477829C>G	GRCh37
NC_000007.12:g.140124298C>G	NCBI36
NG_007873.3:g.151736G>C , LRG_299:g.151736G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1479G>C MANE Select	ENSP00000493543.1:p.Gln493His
ENST00000288602.11:c.1599G>C	ENSP00000288602.7:p.Gln533His
ENST00000479537.6:c.149G>C
ENST00000496384.7:c.1479G>C	ENSP00000419060.2:p.Gln493His
ENST00000497784.2:c.*929G>C	ENSP00000420119.2:n.*929G>C
ENST00000642228.1:c.*557G>C	ENSP00000493678.1:n.*557G>C
ENST00000642875.1:n.1043G>C
ENST00000644120.1:n.1869G>C
ENST00000644650.1:c.575G>C
ENST00000644905.1:n.1568G>C
ENST00000644969.2:c.1599G>C MANE Plus Clinical	ENSP00000496776.1:p.Gln533His
ENST00000646730.1:c.1479G>C	ENSP00000494784.1:p.Gln493His
ENST00000646891.1:c.1479G>C	ENSP00000493543.1:p.Gln493His
ENST00000647434.1:c.522G>C	ENSP00000495132.1:p.Gln174His
ENST00000288602.10:c.1479G>C	ENSP00000288602.6:p.Gln493His
ENST00000496384.6:c.302G>C
ENST00000497784.1:c.1514G>C	ENSP00000420119.1:n.1514G>C
NM_004333.4:c.1479G>C , LRG_299t1:c.1479G>C	NP_004324.2:p.Gln493His
XM_005250045.1:c.1479G>C	XP_005250102.1:p.Gln493His
XM_005250046.1:c.1479G>C	XP_005250103.1:p.Gln493His
XM_011516529.1:c.1479G>C	XP_011514831.1:p.Gln493His
XM_011516530.1:c.1479G>C	XP_011514832.1:p.Gln493His
XR_242190.1:n.1487G>C
XR_927520.1:n.1487G>C
XR_927521.1:n.1487G>C
XR_927522.1:n.1487G>C
XR_927523.1:n.1487G>C
NM_001354609.1:c.1479G>C	NP_001341538.1:p.Gln493His
NM_004333.5:c.1479G>C	NP_004324.2:p.Gln493His
NR_148928.1:n.1784G>C
XM_017012558.1:c.1599G>C	XP_016868047.1:p.Gln533His
XM_017012559.1:c.1599G>C	XP_016868048.1:p.Gln533His
XR_001744857.1:n.1607G>C
XR_001744858.1:n.1607G>C
NM_001354609.2:c.1479G>C	NP_001341538.1:p.Gln493His
NM_001374244.1:c.1599G>C	NP_001361173.1:p.Gln533His
NM_001374258.1:c.1599G>C MANE Plus Clinical	NP_001361187.1:p.Gln533His
NM_004333.6:c.1479G>C MANE Select	NP_004324.2:p.Gln493His
NM_001378467.1:c.1488G>C	NP_001365396.1:p.Gln496His
NM_001378468.1:c.1479G>C	NP_001365397.1:p.Gln493His
NM_001378469.1:c.1413G>C	NP_001365398.1:p.Gln471His
NM_001378470.1:c.1377G>C	NP_001365399.1:p.Gln459His
NM_001378471.1:c.1368G>C	NP_001365400.1:p.Gln456His
NM_001378472.1:c.1323G>C	NP_001365401.1:p.Gln441His
NM_001378473.1:c.1323G>C	NP_001365402.1:p.Gln441His
NM_001378474.1:c.1479G>C	NP_001365403.1:p.Gln493His
NM_001378475.1:c.1215G>C	NP_001365404.1:p.Gln405His