Canonical Allele Identifier: CA10590388

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 868567
• ClinVar RCV Id: RCV001077491
• dbSNP Id: rs398122700
• MyVariant Identifiers: chr17:g.41197814C>G (hg19) ; chr17:g.43045797C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43045797C>G , CM000679.2:g.43045797C>G	GRCh38
NC_000017.10:g.41197814C>G , CM000679.1:g.41197814C>G	GRCh37
NC_000017.9:g.38451340C>G	NCBI36
NG_005905.2:g.172187G>C , LRG_292:g.172187G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5470G>C	ENSP00000417241.2:p.Gly1824Arg
ENST00000470026.6:c.5473G>C	ENSP00000419274.2:p.Gly1825Arg
ENST00000473961.6:c.5347G>C	ENSP00000420201.2:p.Gly1783Arg
ENST00000476777.6:c.5467G>C	ENSP00000417554.2:p.Gly1823Arg
ENST00000477152.6:c.5395G>C	ENSP00000419988.2:p.Gly1799Arg
ENST00000478531.6:c.2161G>C	ENSP00000420412.2:p.Gly721Arg
ENST00000489037.2:c.5395G>C	ENSP00000420781.2:p.Gly1799Arg
ENST00000493919.6:c.2023G>C	ENSP00000418819.2:p.Gly675Arg
ENST00000494123.6:c.5473G>C	ENSP00000419103.2:p.Gly1825Arg
ENST00000497488.2:c.4585G>C	ENSP00000418986.2:p.Gly1529Arg
ENST00000618469.2:c.5473G>C	ENSP00000478114.2:p.Gly1825Arg
ENST00000634433.2:c.5350G>C	ENSP00000489431.2:p.Gly1784Arg
ENST00000644379.2:c.5539G>C	ENSP00000496570.2:p.Gly1847Arg
ENST00000644555.2:c.2023G>C	ENSP00000494614.2:p.Gly675Arg
ENST00000652672.2:c.5332G>C	ENSP00000498906.2:p.Gly1778Arg
ENST00000484087.6:c.2035G>C	ENSP00000419481.2:p.Gly679Arg
ENST00000700081.1:n.1356G>C
ENST00000700082.1:n.837G>C
ENST00000357654.9:c.5473G>C MANE Select	ENSP00000350283.3:p.Gly1825Arg
ENST00000471181.7:c.5536G>C	ENSP00000418960.2:p.Gly1846Arg
ENST00000644379.1:c.1860G>C
ENST00000352993.7:c.2047G>C	ENSP00000312236.5:p.Gly683Arg
ENST00000357654.7:c.5473G>C	ENSP00000350283.3:p.Gly1825Arg
ENST00000461221.5:c.*5256G>C	ENSP00000418548.1:n.*5256G>C
ENST00000468300.5:c.2087G>C	ENSP00000417148.1:p.Trp696Ser
ENST00000471181.6:c.5536G>C	ENSP00000418960.2:p.Gly1846Arg
ENST00000491747.6:c.2161G>C	ENSP00000420705.2:p.Gly721Arg
ENST00000493795.5:c.5332G>C	ENSP00000418775.1:p.Gly1778Arg
ENST00000586385.5:c.403G>C	ENSP00000465818.1:p.Gly135Arg
ENST00000591534.5:c.946G>C	ENSP00000467329.1:p.Gly316Arg
ENST00000591849.5:c.172G>C	ENSP00000465347.1:p.Gly58Arg
NM_007294.3:c.5473G>C , LRG_292t1:c.5473G>C	NP_009225.1:p.Gly1825Arg
NM_007297.3:c.5332G>C	NP_009228.2:p.Gly1778Arg
NM_007298.3:c.2161G>C	NP_009229.2:p.Gly721Arg
NM_007299.3:c.2087G>C	NP_009230.2:p.Trp696Ser
NM_007300.3:c.5536G>C	NP_009231.2:p.Gly1846Arg
NR_027676.1:n.5609G>C
NM_007294.4:c.5473G>C MANE Select	NP_009225.1:p.Gly1825Arg
NM_007297.4:c.5332G>C	NP_009228.2:p.Gly1778Arg
NM_007299.4:c.2087G>C	NP_009230.2:p.Trp696Ser
NM_007300.4:c.5536G>C	NP_009231.2:p.Gly1846Arg
NR_027676.2:n.5650G>C