Canonical Allele Identifier: CA10591567

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 868472
• ClinVar RCV Id: RCV001077379
• dbSNP Id: rs2052356167
• MyVariant Identifiers: chr17:g.41222952T>A (hg19) ; chr17:g.43070935T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43070935T>A , CM000679.2:g.43070935T>A	GRCh38
NC_000017.10:g.41222952T>A , CM000679.1:g.41222952T>A	GRCh37
NC_000017.9:g.38476478T>A	NCBI36
NG_005905.2:g.147049A>T , LRG_292:g.147049A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4976A>T	ENSP00000417241.2:p.Glu1659Val
ENST00000470026.6:c.4979A>T	ENSP00000419274.2:p.Glu1660Val
ENST00000473961.6:c.4853A>T	ENSP00000420201.2:p.Glu1618Val
ENST00000476777.6:c.4973A>T	ENSP00000417554.2:p.Glu1658Val
ENST00000477152.6:c.4901A>T	ENSP00000419988.2:p.Glu1634Val
ENST00000478531.6:c.1667A>T	ENSP00000420412.2:p.Glu556Val
ENST00000489037.2:c.4901A>T	ENSP00000420781.2:p.Glu1634Val
ENST00000493919.6:c.1529A>T	ENSP00000418819.2:p.Glu510Val
ENST00000494123.6:c.4979A>T	ENSP00000419103.2:p.Glu1660Val
ENST00000497488.2:c.4091A>T	ENSP00000418986.2:p.Glu1364Val
ENST00000618469.2:c.4979A>T	ENSP00000478114.2:p.Glu1660Val
ENST00000634433.2:c.4856A>T	ENSP00000489431.2:p.Glu1619Val
ENST00000644379.2:c.5045A>T	ENSP00000496570.2:p.Glu1682Val
ENST00000644555.2:c.1529A>T	ENSP00000494614.2:p.Glu510Val
ENST00000652672.2:c.4838A>T	ENSP00000498906.2:p.Glu1613Val
ENST00000484087.6:c.1541A>T	ENSP00000419481.2:p.Glu514Val
ENST00000700182.1:c.1586A>T	ENSP00000514849.1:p.Glu529Val
ENST00000357654.9:c.4979A>T MANE Select	ENSP00000350283.3:p.Glu1660Val
ENST00000471181.7:c.5042A>T	ENSP00000418960.2:p.Glu1681Val
ENST00000644379.1:c.1366A>T
ENST00000352993.7:c.1553A>T	ENSP00000312236.5:p.Glu518Val
ENST00000357654.7:c.4979A>T	ENSP00000350283.3:p.Glu1660Val
ENST00000461221.5:c.*4762A>T	ENSP00000418548.1:n.*4762A>T
ENST00000468300.5:c.1667A>T	ENSP00000417148.1:p.Glu556Val
ENST00000471181.6:c.5042A>T	ENSP00000418960.2:p.Glu1681Val
ENST00000472490.1:n.132A>T
ENST00000478531.5:c.1667A>T	ENSP00000420412.1:p.Glu556Val
ENST00000484087.5:c.1292A>T	ENSP00000419481.1:p.Glu431Val
ENST00000491747.6:c.1667A>T	ENSP00000420705.2:p.Glu556Val
ENST00000493795.5:c.4838A>T	ENSP00000418775.1:p.Glu1613Val
ENST00000493919.5:c.1529A>T	ENSP00000418819.1:p.Glu510Val
ENST00000586385.5:c.5-6984A>T	ENSP00000465818.1:n.5-6984A>T
ENST00000591534.5:c.452A>T	ENSP00000467329.1:p.Glu151Val
ENST00000591849.5:c.-98-20745A>T	ENSP00000465347.1:n.-98-20745A>T
NM_007294.3:c.4979A>T , LRG_292t1:c.4979A>T	NP_009225.1:p.Glu1660Val
NM_007297.3:c.4838A>T	NP_009228.2:p.Glu1613Val
NM_007298.3:c.1667A>T	NP_009229.2:p.Glu556Val
NM_007299.3:c.1667A>T	NP_009230.2:p.Glu556Val
NM_007300.3:c.5042A>T	NP_009231.2:p.Glu1681Val
NR_027676.1:n.5115A>T
NM_007294.4:c.4979A>T MANE Select	NP_009225.1:p.Glu1660Val
NM_007297.4:c.4838A>T	NP_009228.2:p.Glu1613Val
NM_007299.4:c.1667A>T	NP_009230.2:p.Glu556Val
NM_007300.4:c.5042A>T	NP_009231.2:p.Glu1681Val
NR_027676.2:n.5156A>T