Canonical Allele Identifier: CA003153

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 141076
• ClinVar RCV Id: RCV000129426 ; RCV000793966 ; RCV001077924 ; RCV003477540
• dbSNP Id: rs587781477
• MyVariant Identifiers: chr17:g.41219685G>A (hg19) ; chr17:g.43067668G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067668G>A , CM000679.2:g.43067668G>A	GRCh38
NC_000017.10:g.41219685G>A , CM000679.1:g.41219685G>A	GRCh37
NC_000017.9:g.38473211G>A	NCBI36
NG_005905.2:g.150316C>T , LRG_292:g.150316C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5011C>T	ENSP00000417241.2:p.His1671Tyr
ENST00000470026.6:c.5014C>T	ENSP00000419274.2:p.His1672Tyr
ENST00000473961.6:c.4888C>T	ENSP00000420201.2:p.His1630Tyr
ENST00000476777.6:c.5008C>T	ENSP00000417554.2:p.His1670Tyr
ENST00000477152.6:c.4936C>T	ENSP00000419988.2:p.His1646Tyr
ENST00000478531.6:c.1702C>T	ENSP00000420412.2:p.His568Tyr
ENST00000489037.2:c.4936C>T	ENSP00000420781.2:p.His1646Tyr
ENST00000493919.6:c.1564C>T	ENSP00000418819.2:p.His522Tyr
ENST00000494123.6:c.5014C>T	ENSP00000419103.2:p.His1672Tyr
ENST00000497488.2:c.4126C>T	ENSP00000418986.2:p.His1376Tyr
ENST00000618469.2:c.5014C>T	ENSP00000478114.2:p.His1672Tyr
ENST00000634433.2:c.4891C>T	ENSP00000489431.2:p.His1631Tyr
ENST00000644379.2:c.5080C>T	ENSP00000496570.2:p.His1694Tyr
ENST00000644555.2:c.1564C>T	ENSP00000494614.2:p.His522Tyr
ENST00000652672.2:c.4873C>T	ENSP00000498906.2:p.His1625Tyr
ENST00000484087.6:c.1576C>T	ENSP00000419481.2:p.His526Tyr
ENST00000357654.9:c.5014C>T MANE Select	ENSP00000350283.3:p.His1672Tyr
ENST00000471181.7:c.5077C>T	ENSP00000418960.2:p.His1693Tyr
ENST00000644379.1:c.1401C>T
ENST00000352993.7:c.1588C>T	ENSP00000312236.5:p.His530Tyr
ENST00000357654.7:c.5014C>T	ENSP00000350283.3:p.His1672Tyr
ENST00000461221.5:c.*4797C>T	ENSP00000418548.1:n.*4797C>T
ENST00000468300.5:c.1702C>T	ENSP00000417148.1:p.His568Tyr
ENST00000471181.6:c.5077C>T	ENSP00000418960.2:p.His1693Tyr
ENST00000472490.1:n.167C>T
ENST00000478531.5:c.1702C>T	ENSP00000420412.1:p.His568Tyr
ENST00000484087.5:c.1327C>T	ENSP00000419481.1:p.His443Tyr
ENST00000491747.6:c.1702C>T	ENSP00000420705.2:p.His568Tyr
ENST00000493795.5:c.4873C>T	ENSP00000418775.1:p.His1625Tyr
ENST00000493919.5:c.1564C>T	ENSP00000418819.1:p.His522Tyr
ENST00000586385.5:c.5-3717C>T	ENSP00000465818.1:n.5-3717C>T
ENST00000591534.5:c.487C>T	ENSP00000467329.1:p.His163Tyr
ENST00000591849.5:c.-98-17478C>T	ENSP00000465347.1:n.-98-17478C>T
NM_007294.3:c.5014C>T , LRG_292t1:c.5014C>T	NP_009225.1:p.His1672Tyr
NM_007297.3:c.4873C>T	NP_009228.2:p.His1625Tyr
NM_007298.3:c.1702C>T	NP_009229.2:p.His568Tyr
NM_007299.3:c.1702C>T	NP_009230.2:p.His568Tyr
NM_007300.3:c.5077C>T	NP_009231.2:p.His1693Tyr
NR_027676.1:n.5150C>T
NM_007294.4:c.5014C>T MANE Select	NP_009225.1:p.His1672Tyr
NM_007297.4:c.4873C>T	NP_009228.2:p.His1625Tyr
NM_007299.4:c.1702C>T	NP_009230.2:p.His568Tyr
NM_007300.4:c.5077C>T	NP_009231.2:p.His1693Tyr
NR_027676.2:n.5191C>T