Canonical Allele Identifier: CA003365

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 55462
• ClinVar RCV Id: RCV000048864 ; RCV000077609 ; RCV001190130 ; RCV003321494
• dbSNP Id: rs80357450
• MyVariant Identifiers: chr17:g.41209133C>T (hg19) ; chr17:g.43057116C>T (hg38)
• PubMed: PMID:17308087 ; PMID:20516115

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43057116C>T , CM000679.2:g.43057116C>T	GRCh38
NC_000017.10:g.41209133C>T , CM000679.1:g.41209133C>T	GRCh37
NC_000017.9:g.38462659C>T	NCBI36
NG_005905.2:g.160868G>A , LRG_292:g.160868G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5210G>A	ENSP00000417241.2:p.Gly1737Glu
ENST00000470026.6:c.5213G>A	ENSP00000419274.2:p.Gly1738Glu
ENST00000473961.6:c.5087G>A	ENSP00000420201.2:p.Gly1696Glu
ENST00000476777.6:c.5207G>A	ENSP00000417554.2:p.Gly1736Glu
ENST00000477152.6:c.5135G>A	ENSP00000419988.2:p.Gly1712Glu
ENST00000478531.6:c.1901G>A	ENSP00000420412.2:p.Gly634Glu
ENST00000489037.2:c.5135G>A	ENSP00000420781.2:p.Gly1712Glu
ENST00000493919.6:c.1763G>A	ENSP00000418819.2:p.Gly588Glu
ENST00000494123.6:c.5213G>A	ENSP00000419103.2:p.Gly1738Glu
ENST00000497488.2:c.4325G>A	ENSP00000418986.2:p.Gly1442Glu
ENST00000618469.2:c.5213G>A	ENSP00000478114.2:p.Gly1738Glu
ENST00000634433.2:c.5090G>A	ENSP00000489431.2:p.Gly1697Glu
ENST00000644379.2:c.5279G>A	ENSP00000496570.2:p.Gly1760Glu
ENST00000644555.2:c.1763G>A	ENSP00000494614.2:p.Gly588Glu
ENST00000652672.2:c.5072G>A	ENSP00000498906.2:p.Gly1691Glu
ENST00000484087.6:c.1775G>A	ENSP00000419481.2:p.Gly592Glu
ENST00000357654.9:c.5213G>A MANE Select	ENSP00000350283.3:p.Gly1738Glu
ENST00000471181.7:c.5276G>A	ENSP00000418960.2:p.Gly1759Glu
ENST00000644379.1:c.1600G>A
ENST00000352993.7:c.1787G>A	ENSP00000312236.5:p.Gly596Glu
ENST00000357654.7:c.5213G>A	ENSP00000350283.3:p.Gly1738Glu
ENST00000461221.5:c.*4996G>A	ENSP00000418548.1:n.*4996G>A
ENST00000468300.5:c.1901G>A	ENSP00000417148.1:p.Gly634Glu
ENST00000471181.6:c.5276G>A	ENSP00000418960.2:p.Gly1759Glu
ENST00000491747.6:c.1901G>A	ENSP00000420705.2:p.Gly634Glu
ENST00000493795.5:c.5072G>A	ENSP00000418775.1:p.Gly1691Glu
ENST00000586385.5:c.143G>A	ENSP00000465818.1:p.Gly48Glu
ENST00000591534.5:c.686G>A	ENSP00000467329.1:p.Gly229Glu
ENST00000591849.5:c.-98-6926G>A	ENSP00000465347.1:n.-98-6926G>A
NM_007294.3:c.5213G>A , LRG_292t1:c.5213G>A	NP_009225.1:p.Gly1738Glu
NM_007297.3:c.5072G>A	NP_009228.2:p.Gly1691Glu
NM_007298.3:c.1901G>A	NP_009229.2:p.Gly634Glu
NM_007299.3:c.1901G>A	NP_009230.2:p.Gly634Glu
NM_007300.3:c.5276G>A	NP_009231.2:p.Gly1759Glu
NR_027676.1:n.5349G>A
NM_007294.4:c.5213G>A MANE Select	NP_009225.1:p.Gly1738Glu
NM_007297.4:c.5072G>A	NP_009228.2:p.Gly1691Glu
NM_007299.4:c.1901G>A	NP_009230.2:p.Gly634Glu
NM_007300.4:c.5276G>A	NP_009231.2:p.Gly1759Glu
NR_027676.2:n.5390G>A