Canonical Allele Identifier: CA10591749

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 487415
• ClinVar RCV Id: RCV000576818 ; RCV002341491 ; RCV001853823
• dbSNP Id: rs1173155015
• MyVariant Identifiers: chr17:g.41223043C>A (hg19) ; chr17:g.43071026C>A (hg38)
• PubMed: PMID:27756336

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43071026C>A , CM000679.2:g.43071026C>A	GRCh38
NC_000017.10:g.41223043C>A , CM000679.1:g.41223043C>A	GRCh37
NC_000017.9:g.38476569C>A	NCBI36
NG_005905.2:g.146958G>T , LRG_292:g.146958G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4885G>T	ENSP00000417241.2:p.Glu1629Ter
ENST00000470026.6:c.4888G>T	ENSP00000419274.2:p.Glu1630Ter
ENST00000473961.6:c.4762G>T	ENSP00000420201.2:p.Glu1588Ter
ENST00000476777.6:c.4882G>T	ENSP00000417554.2:p.Glu1628Ter
ENST00000477152.6:c.4810G>T	ENSP00000419988.2:p.Glu1604Ter
ENST00000478531.6:c.1576G>T	ENSP00000420412.2:p.Glu526Ter
ENST00000489037.2:c.4810G>T	ENSP00000420781.2:p.Glu1604Ter
ENST00000493919.6:c.1438G>T	ENSP00000418819.2:p.Glu480Ter
ENST00000494123.6:c.4888G>T	ENSP00000419103.2:p.Glu1630Ter
ENST00000497488.2:c.4000G>T	ENSP00000418986.2:p.Glu1334Ter
ENST00000618469.2:c.4888G>T	ENSP00000478114.2:p.Glu1630Ter
ENST00000634433.2:c.4765G>T	ENSP00000489431.2:p.Glu1589Ter
ENST00000644379.2:c.4954G>T	ENSP00000496570.2:p.Glu1652Ter
ENST00000644555.2:c.1438G>T	ENSP00000494614.2:p.Glu480Ter
ENST00000652672.2:c.4747G>T	ENSP00000498906.2:p.Glu1583Ter
ENST00000484087.6:c.1450G>T	ENSP00000419481.2:p.Glu484Ter
ENST00000700182.1:c.1495G>T	ENSP00000514849.1:p.Glu499Ter
ENST00000357654.9:c.4888G>T MANE Select	ENSP00000350283.3:p.Glu1630Ter
ENST00000471181.7:c.4951G>T	ENSP00000418960.2:p.Glu1651Ter
ENST00000644379.1:c.1275G>T
ENST00000352993.7:c.1462G>T	ENSP00000312236.5:p.Glu488Ter
ENST00000357654.7:c.4888G>T	ENSP00000350283.3:p.Glu1630Ter
ENST00000461221.5:c.*4671G>T	ENSP00000418548.1:n.*4671G>T
ENST00000468300.5:c.1576G>T	ENSP00000417148.1:p.Glu526Ter
ENST00000471181.6:c.4951G>T	ENSP00000418960.2:p.Glu1651Ter
ENST00000472490.1:n.41G>T
ENST00000478531.5:c.1576G>T	ENSP00000420412.1:p.Glu526Ter
ENST00000484087.5:c.1201G>T	ENSP00000419481.1:p.Glu401Ter
ENST00000491747.6:c.1576G>T	ENSP00000420705.2:p.Glu526Ter
ENST00000493795.5:c.4747G>T	ENSP00000418775.1:p.Glu1583Ter
ENST00000493919.5:c.1438G>T	ENSP00000418819.1:p.Glu480Ter
ENST00000586385.5:c.5-7075G>T	ENSP00000465818.1:n.5-7075G>T
ENST00000591534.5:c.361G>T	ENSP00000467329.1:p.Glu121Ter
ENST00000591849.5:c.-98-20836G>T	ENSP00000465347.1:n.-98-20836G>T
NM_007294.3:c.4888G>T , LRG_292t1:c.4888G>T	NP_009225.1:p.Glu1630Ter
NM_007297.3:c.4747G>T	NP_009228.2:p.Glu1583Ter
NM_007298.3:c.1576G>T	NP_009229.2:p.Glu526Ter
NM_007299.3:c.1576G>T	NP_009230.2:p.Glu526Ter
NM_007300.3:c.4951G>T	NP_009231.2:p.Glu1651Ter
NR_027676.1:n.5024G>T
NM_007294.4:c.4888G>T MANE Select	NP_009225.1:p.Glu1630Ter
NM_007297.4:c.4747G>T	NP_009228.2:p.Glu1583Ter
NM_007299.4:c.1576G>T	NP_009230.2:p.Glu526Ter
NM_007300.4:c.4951G>T	NP_009231.2:p.Glu1651Ter
NR_027676.2:n.5065G>T