Canonical Allele Identifier: CA10592567

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 2836927
• ClinVar RCV Id: RCV003645815
• MyVariant Identifiers: chr17:g.41228506T>A (hg19) ; chr17:g.43076489T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076489T>A , CM000679.2:g.43076489T>A	GRCh38
NC_000017.10:g.41228506T>A , CM000679.1:g.41228506T>A	GRCh37
NC_000017.9:g.38482032T>A	NCBI36
NG_005905.2:g.141495A>T , LRG_292:g.141495A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4480A>T	ENSP00000417241.2:p.Arg1494Trp
ENST00000470026.6:c.4483A>T	ENSP00000419274.2:p.Arg1495Trp
ENST00000473961.6:c.4357A>T	ENSP00000420201.2:p.Arg1453Trp
ENST00000476777.6:c.4477A>T	ENSP00000417554.2:p.Arg1493Trp
ENST00000477152.6:c.4405A>T	ENSP00000419988.2:p.Arg1469Trp
ENST00000478531.6:c.1171A>T	ENSP00000420412.2:p.Arg391Trp
ENST00000489037.2:c.4405A>T	ENSP00000420781.2:p.Arg1469Trp
ENST00000493919.6:c.1033A>T	ENSP00000418819.2:p.Arg345Trp
ENST00000494123.6:c.4483A>T	ENSP00000419103.2:p.Arg1495Trp
ENST00000497488.2:c.3595A>T	ENSP00000418986.2:p.Arg1199Trp
ENST00000618469.2:c.4483A>T	ENSP00000478114.2:p.Arg1495Trp
ENST00000634433.2:c.4360A>T	ENSP00000489431.2:p.Arg1454Trp
ENST00000644379.2:c.4549A>T	ENSP00000496570.2:p.Arg1517Trp
ENST00000644555.2:c.1033A>T	ENSP00000494614.2:p.Arg345Trp
ENST00000652672.2:c.4342A>T	ENSP00000498906.2:p.Arg1448Trp
ENST00000484087.6:c.1045A>T	ENSP00000419481.2:p.Arg349Trp
ENST00000700182.1:c.1090A>T	ENSP00000514849.1:p.Arg364Trp
ENST00000357654.9:c.4483A>T MANE Select	ENSP00000350283.3:p.Arg1495Trp
ENST00000471181.7:c.4546A>T	ENSP00000418960.2:p.Arg1516Trp
ENST00000644379.1:c.870A>T
ENST00000352993.7:c.1057A>T	ENSP00000312236.5:p.Arg353Trp
ENST00000357654.7:c.4483A>T	ENSP00000350283.3:p.Arg1495Trp
ENST00000461221.5:c.*4266A>T	ENSP00000418548.1:n.*4266A>T
ENST00000468300.5:c.1171A>T	ENSP00000417148.1:p.Arg391Trp
ENST00000471181.6:c.4546A>T	ENSP00000418960.2:p.Arg1516Trp
ENST00000478531.5:c.1171A>T	ENSP00000420412.1:p.Arg391Trp
ENST00000484087.5:c.796A>T	ENSP00000419481.1:p.Arg266Trp
ENST00000487825.5:c.799A>T
ENST00000491747.6:c.1171A>T	ENSP00000420705.2:p.Arg391Trp
ENST00000493795.5:c.4342A>T	ENSP00000418775.1:p.Arg1448Trp
ENST00000493919.5:c.1033A>T	ENSP00000418819.1:p.Arg345Trp
ENST00000586385.5:c.5-12538A>T	ENSP00000465818.1:n.5-12538A>T
ENST00000591534.5:c.-43-1968A>T	ENSP00000467329.1:n.-43-1968A>T
ENST00000591849.5:c.-98-26299A>T	ENSP00000465347.1:n.-98-26299A>T
ENST00000621897.1:n.374A>T
NM_007294.3:c.4483A>T , LRG_292t1:c.4483A>T	NP_009225.1:p.Arg1495Trp
NM_007297.3:c.4342A>T	NP_009228.2:p.Arg1448Trp
NM_007298.3:c.1171A>T	NP_009229.2:p.Arg391Trp
NM_007299.3:c.1171A>T	NP_009230.2:p.Arg391Trp
NM_007300.3:c.4546A>T	NP_009231.2:p.Arg1516Trp
NR_027676.1:n.4619A>T
NM_007294.4:c.4483A>T MANE Select	NP_009225.1:p.Arg1495Trp
NM_007297.4:c.4342A>T	NP_009228.2:p.Arg1448Trp
NM_007299.4:c.1171A>T	NP_009230.2:p.Arg391Trp
NM_007300.4:c.4546A>T	NP_009231.2:p.Arg1516Trp
NR_027676.2:n.4660A>T