Canonical Allele Identifier: CA369588848

Gene: BRAF

Linked Data

• dbSNP Id: rs2129023492
• MyVariant Identifiers: chr7:g.140481387C>G (hg19) ; chr7:g.140781587C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781587C>G , CM000669.2:g.140781587C>G	GRCh38
NC_000007.13:g.140481387C>G , CM000669.1:g.140481387C>G	GRCh37
NC_000007.12:g.140127856C>G	NCBI36
NG_007873.3:g.148178G>C , LRG_299:g.148178G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1421G>C MANE Select	ENSP00000493543.1:p.Gly474Ala
ENST00000288602.11:c.1541G>C	ENSP00000288602.7:p.Gly514Ala
ENST00000479537.6:c.91G>C
ENST00000496384.7:c.1421G>C	ENSP00000419060.2:p.Gly474Ala
ENST00000497784.2:c.*871G>C	ENSP00000420119.2:n.*871G>C
ENST00000642228.1:c.*499G>C	ENSP00000493678.1:n.*499G>C
ENST00000642875.1:n.863G>C
ENST00000644120.1:n.1811G>C
ENST00000644650.1:c.517G>C
ENST00000644905.1:n.1510G>C
ENST00000644969.2:c.1541G>C MANE Plus Clinical	ENSP00000496776.1:p.Gly514Ala
ENST00000646334.1:n.551G>C
ENST00000646730.1:c.1421G>C	ENSP00000494784.1:p.Gly474Ala
ENST00000646891.1:c.1421G>C	ENSP00000493543.1:p.Gly474Ala
ENST00000647434.1:c.464G>C	ENSP00000495132.1:p.Gly155Ala
ENST00000288602.10:c.1421G>C	ENSP00000288602.6:p.Gly474Ala
ENST00000496384.6:c.244G>C
ENST00000497784.1:c.1456G>C	ENSP00000420119.1:n.1456G>C
NM_004333.4:c.1421G>C , LRG_299t1:c.1421G>C	NP_004324.2:p.Gly474Ala
XM_005250045.1:c.1421G>C	XP_005250102.1:p.Gly474Ala
XM_005250046.1:c.1421G>C	XP_005250103.1:p.Gly474Ala
XM_011516529.1:c.1421G>C	XP_011514831.1:p.Gly474Ala
XM_011516530.1:c.1421G>C	XP_011514832.1:p.Gly474Ala
XR_242190.1:n.1429G>C
XR_927520.1:n.1429G>C
XR_927521.1:n.1429G>C
XR_927522.1:n.1429G>C
XR_927523.1:n.1429G>C
NM_001354609.1:c.1421G>C	NP_001341538.1:p.Gly474Ala
NM_004333.5:c.1421G>C	NP_004324.2:p.Gly474Ala
NR_148928.1:n.1726G>C
XM_017012558.1:c.1541G>C	XP_016868047.1:p.Gly514Ala
XM_017012559.1:c.1541G>C	XP_016868048.1:p.Gly514Ala
XR_001744857.1:n.1549G>C
XR_001744858.1:n.1549G>C
NM_001354609.2:c.1421G>C	NP_001341538.1:p.Gly474Ala
NM_001374244.1:c.1541G>C	NP_001361173.1:p.Gly514Ala
NM_001374258.1:c.1541G>C MANE Plus Clinical	NP_001361187.1:p.Gly514Ala
NM_004333.6:c.1421G>C MANE Select	NP_004324.2:p.Gly474Ala
NM_001378467.1:c.1430G>C	NP_001365396.1:p.Gly477Ala
NM_001378468.1:c.1421G>C	NP_001365397.1:p.Gly474Ala
NM_001378469.1:c.1355G>C	NP_001365398.1:p.Gly452Ala
NM_001378470.1:c.1319G>C	NP_001365399.1:p.Gly440Ala
NM_001378471.1:c.1310G>C	NP_001365400.1:p.Gly437Ala
NM_001378472.1:c.1265G>C	NP_001365401.1:p.Gly422Ala
NM_001378473.1:c.1265G>C	NP_001365402.1:p.Gly422Ala
NM_001378474.1:c.1421G>C	NP_001365403.1:p.Gly474Ala
NM_001378475.1:c.1157G>C	NP_001365404.1:p.Gly386Ala