Canonical Allele Identifier: CA10592590

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 482951
• ClinVar RCV Id: RCV000573390
• dbSNP Id: rs1555582549
• MyVariant Identifiers: chr17:g.41228519T>A (hg19) ; chr17:g.43076502T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076502T>A , CM000679.2:g.43076502T>A	GRCh38
NC_000017.10:g.41228519T>A , CM000679.1:g.41228519T>A	GRCh37
NC_000017.9:g.38482045T>A	NCBI36
NG_005905.2:g.141482A>T , LRG_292:g.141482A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4467A>T	ENSP00000417241.2:p.Glu1489Asp
ENST00000470026.6:c.4470A>T	ENSP00000419274.2:p.Glu1490Asp
ENST00000473961.6:c.4344A>T	ENSP00000420201.2:p.Glu1448Asp
ENST00000476777.6:c.4464A>T	ENSP00000417554.2:p.Glu1488Asp
ENST00000477152.6:c.4392A>T	ENSP00000419988.2:p.Glu1464Asp
ENST00000478531.6:c.1158A>T	ENSP00000420412.2:p.Glu386Asp
ENST00000489037.2:c.4392A>T	ENSP00000420781.2:p.Glu1464Asp
ENST00000493919.6:c.1020A>T	ENSP00000418819.2:p.Glu340Asp
ENST00000494123.6:c.4470A>T	ENSP00000419103.2:p.Glu1490Asp
ENST00000497488.2:c.3582A>T	ENSP00000418986.2:p.Glu1194Asp
ENST00000618469.2:c.4470A>T	ENSP00000478114.2:p.Glu1490Asp
ENST00000634433.2:c.4347A>T	ENSP00000489431.2:p.Glu1449Asp
ENST00000644379.2:c.4536A>T	ENSP00000496570.2:p.Glu1512Asp
ENST00000644555.2:c.1020A>T	ENSP00000494614.2:p.Glu340Asp
ENST00000652672.2:c.4329A>T	ENSP00000498906.2:p.Glu1443Asp
ENST00000484087.6:c.1032A>T	ENSP00000419481.2:p.Glu344Asp
ENST00000700182.1:c.1077A>T	ENSP00000514849.1:p.Glu359Asp
ENST00000357654.9:c.4470A>T MANE Select	ENSP00000350283.3:p.Glu1490Asp
ENST00000471181.7:c.4533A>T	ENSP00000418960.2:p.Glu1511Asp
ENST00000644379.1:c.857A>T
ENST00000352993.7:c.1044A>T	ENSP00000312236.5:p.Glu348Asp
ENST00000357654.7:c.4470A>T	ENSP00000350283.3:p.Glu1490Asp
ENST00000461221.5:c.*4253A>T	ENSP00000418548.1:n.*4253A>T
ENST00000468300.5:c.1158A>T	ENSP00000417148.1:p.Glu386Asp
ENST00000471181.6:c.4533A>T	ENSP00000418960.2:p.Glu1511Asp
ENST00000478531.5:c.1158A>T	ENSP00000420412.1:p.Glu386Asp
ENST00000484087.5:c.783A>T	ENSP00000419481.1:p.Glu261Asp
ENST00000487825.5:c.786A>T	ENSP00000418212.1:p.Glu262Asp
ENST00000491747.6:c.1158A>T	ENSP00000420705.2:p.Glu386Asp
ENST00000493795.5:c.4329A>T	ENSP00000418775.1:p.Glu1443Asp
ENST00000493919.5:c.1020A>T	ENSP00000418819.1:p.Glu340Asp
ENST00000586385.5:c.5-12551A>T	ENSP00000465818.1:n.5-12551A>T
ENST00000591534.5:c.-43-1981A>T	ENSP00000467329.1:n.-43-1981A>T
ENST00000591849.5:c.-98-26312A>T	ENSP00000465347.1:n.-98-26312A>T
ENST00000621897.1:n.361A>T
NM_007294.3:c.4470A>T , LRG_292t1:c.4470A>T	NP_009225.1:p.Glu1490Asp
NM_007297.3:c.4329A>T	NP_009228.2:p.Glu1443Asp
NM_007298.3:c.1158A>T	NP_009229.2:p.Glu386Asp
NM_007299.3:c.1158A>T	NP_009230.2:p.Glu386Asp
NM_007300.3:c.4533A>T	NP_009231.2:p.Glu1511Asp
NR_027676.1:n.4606A>T
NM_007294.4:c.4470A>T MANE Select	NP_009225.1:p.Glu1490Asp
NM_007297.4:c.4329A>T	NP_009228.2:p.Glu1443Asp
NM_007299.4:c.1158A>T	NP_009230.2:p.Glu386Asp
NM_007300.4:c.4533A>T	NP_009231.2:p.Glu1511Asp
NR_027676.2:n.4647A>T