Canonical Allele Identifier: CA10591114

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 865165
• ClinVar RCV Id: RCV001072528 ; RCV001177964
• dbSNP Id: rs80356937
• MyVariant Identifiers: chr17:g.41209134C>G (hg19) ; chr17:g.43057117C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43057117C>G , CM000679.2:g.43057117C>G	GRCh38
NC_000017.10:g.41209134C>G , CM000679.1:g.41209134C>G	GRCh37
NC_000017.9:g.38462660C>G	NCBI36
NG_005905.2:g.160867G>C , LRG_292:g.160867G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5209G>C	ENSP00000417241.2:p.Gly1737Arg
ENST00000470026.6:c.5212G>C	ENSP00000419274.2:p.Gly1738Arg
ENST00000473961.6:c.5086G>C	ENSP00000420201.2:p.Gly1696Arg
ENST00000476777.6:c.5206G>C	ENSP00000417554.2:p.Gly1736Arg
ENST00000477152.6:c.5134G>C	ENSP00000419988.2:p.Gly1712Arg
ENST00000478531.6:c.1900G>C	ENSP00000420412.2:p.Gly634Arg
ENST00000489037.2:c.5134G>C	ENSP00000420781.2:p.Gly1712Arg
ENST00000493919.6:c.1762G>C	ENSP00000418819.2:p.Gly588Arg
ENST00000494123.6:c.5212G>C	ENSP00000419103.2:p.Gly1738Arg
ENST00000497488.2:c.4324G>C	ENSP00000418986.2:p.Gly1442Arg
ENST00000618469.2:c.5212G>C	ENSP00000478114.2:p.Gly1738Arg
ENST00000634433.2:c.5089G>C	ENSP00000489431.2:p.Gly1697Arg
ENST00000644379.2:c.5278G>C	ENSP00000496570.2:p.Gly1760Arg
ENST00000644555.2:c.1762G>C	ENSP00000494614.2:p.Gly588Arg
ENST00000652672.2:c.5071G>C	ENSP00000498906.2:p.Gly1691Arg
ENST00000484087.6:c.1774G>C	ENSP00000419481.2:p.Gly592Arg
ENST00000357654.9:c.5212G>C MANE Select	ENSP00000350283.3:p.Gly1738Arg
ENST00000471181.7:c.5275G>C	ENSP00000418960.2:p.Gly1759Arg
ENST00000644379.1:c.1599G>C
ENST00000352993.7:c.1786G>C	ENSP00000312236.5:p.Gly596Arg
ENST00000357654.7:c.5212G>C	ENSP00000350283.3:p.Gly1738Arg
ENST00000461221.5:c.*4995G>C	ENSP00000418548.1:n.*4995G>C
ENST00000468300.5:c.1900G>C	ENSP00000417148.1:p.Gly634Arg
ENST00000471181.6:c.5275G>C	ENSP00000418960.2:p.Gly1759Arg
ENST00000491747.6:c.1900G>C	ENSP00000420705.2:p.Gly634Arg
ENST00000493795.5:c.5071G>C	ENSP00000418775.1:p.Gly1691Arg
ENST00000586385.5:c.142G>C	ENSP00000465818.1:p.Gly48Arg
ENST00000591534.5:c.685G>C	ENSP00000467329.1:p.Gly229Arg
ENST00000591849.5:c.-98-6927G>C	ENSP00000465347.1:n.-98-6927G>C
NM_007294.3:c.5212G>C , LRG_292t1:c.5212G>C	NP_009225.1:p.Gly1738Arg
NM_007297.3:c.5071G>C	NP_009228.2:p.Gly1691Arg
NM_007298.3:c.1900G>C	NP_009229.2:p.Gly634Arg
NM_007299.3:c.1900G>C	NP_009230.2:p.Gly634Arg
NM_007300.3:c.5275G>C	NP_009231.2:p.Gly1759Arg
NR_027676.1:n.5348G>C
NM_007294.4:c.5212G>C MANE Select	NP_009225.1:p.Gly1738Arg
NM_007297.4:c.5071G>C	NP_009228.2:p.Gly1691Arg
NM_007299.4:c.1900G>C	NP_009230.2:p.Gly634Arg
NM_007300.4:c.5275G>C	NP_009231.2:p.Gly1759Arg
NR_027676.2:n.5389G>C