Canonical Allele Identifier: CA10600171

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 482897
• ClinVar RCV Id: RCV000561351 ; RCV001055289 ; RCV001584381 ; RCV004001007
• dbSNP Id: rs1555592782
• MyVariant Identifiers: chr17:g.41246600G>C (hg19) ; chr17:g.43094583G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094583G>C , CM000679.2:g.43094583G>C	GRCh38
NC_000017.10:g.41246600G>C , CM000679.1:g.41246600G>C	GRCh37
NC_000017.9:g.38500126G>C	NCBI36
NG_005905.2:g.123401C>G , LRG_292:g.123401C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1012C>G
ENST00000461574.2:c.948C>G	ENSP00000417241.2:p.Ser316Arg
ENST00000470026.6:c.948C>G	ENSP00000419274.2:p.Ser316Arg
ENST00000473961.6:c.822C>G	ENSP00000420201.2:p.Ser274Arg
ENST00000476777.6:c.945C>G	ENSP00000417554.2:p.Ser315Arg
ENST00000477152.6:c.870C>G	ENSP00000419988.2:p.Ser290Arg
ENST00000478531.6:c.784+161C>G	ENSP00000420412.2:n.784+161C>G
ENST00000489037.2:c.870C>G	ENSP00000420781.2:p.Ser290Arg
ENST00000493919.6:c.646+161C>G	ENSP00000418819.2:n.646+161C>G
ENST00000494123.6:c.948C>G	ENSP00000419103.2:p.Ser316Arg
ENST00000497488.2:c.60C>G	ENSP00000418986.2:p.Ser20Arg
ENST00000618469.2:c.948C>G	ENSP00000478114.2:p.Ser316Arg
ENST00000634433.2:c.825C>G	ENSP00000489431.2:p.Ser275Arg
ENST00000644379.2:c.948C>G	ENSP00000496570.2:p.Ser316Arg
ENST00000644555.2:c.646+161C>G	ENSP00000494614.2:n.646+161C>G
ENST00000652672.2:c.807C>G	ENSP00000498906.2:p.Ser269Arg
ENST00000484087.6:c.664+161C>G	ENSP00000419481.2:n.664+161C>G
ENST00000700182.1:c.706+161C>G	ENSP00000514849.1:n.706+161C>G
ENST00000700183.1:c.*956C>G	ENSP00000514850.1:n.*956C>G
ENST00000357654.9:c.948C>G MANE Select	ENSP00000350283.3:p.Ser316Arg
ENST00000471181.7:c.948C>G	ENSP00000418960.2:p.Ser316Arg
ENST00000642945.1:c.*822C>G	ENSP00000495897.1:n.*822C>G
ENST00000652672.1:c.807C>G	ENSP00000498906.1:p.Ser269Arg
ENST00000352993.7:c.670+1263C>G	ENSP00000312236.5:n.670+1263C>G
ENST00000354071.7:c.948C>G	ENSP00000326002.7:p.Ser316Arg
ENST00000357654.7:c.948C>G	ENSP00000350283.3:p.Ser316Arg
ENST00000412061.3:c.299C>G
ENST00000461221.5:c.*731C>G	ENSP00000418548.1:n.*731C>G
ENST00000468300.5:c.787+161C>G	ENSP00000417148.1:n.787+161C>G
ENST00000470026.5:c.948C>G	ENSP00000419274.1:p.Ser316Arg
ENST00000471181.6:c.948C>G	ENSP00000418960.2:p.Ser316Arg
ENST00000473961.5:c.545C>G
ENST00000477152.5:c.870C>G	ENSP00000419988.1:p.Ser290Arg
ENST00000478531.5:c.784+161C>G	ENSP00000420412.1:n.784+161C>G
ENST00000484087.5:c.409+161C>G	ENSP00000419481.1:n.409+161C>G
ENST00000487825.5:c.412+161C>G	ENSP00000418212.1:n.412+161C>G
ENST00000491747.6:c.787+161C>G	ENSP00000420705.2:n.787+161C>G
ENST00000492859.5:c.*884C>G	ENSP00000420253.1:n.*884C>G
ENST00000493795.5:c.807C>G	ENSP00000418775.1:p.Ser269Arg
ENST00000493919.5:c.646+161C>G	ENSP00000418819.1:n.646+161C>G
ENST00000494123.5:c.948C>G	ENSP00000419103.1:p.Ser316Arg
ENST00000497488.1:c.60C>G	ENSP00000418986.1:p.Ser20Arg
ENST00000586385.5:c.4+30599C>G	ENSP00000465818.1:n.4+30599C>G
ENST00000591534.5:c.-43-20062C>G	ENSP00000467329.1:n.-43-20062C>G
ENST00000591849.5:c.-99+30688C>G	ENSP00000465347.1:n.-99+30688C>G
ENST00000634433.1:c.825C>G	ENSP00000489431.1:p.Ser275Arg
NM_007294.3:c.948C>G , LRG_292t1:c.948C>G	NP_009225.1:p.Ser316Arg
NM_007297.3:c.807C>G	NP_009228.2:p.Ser269Arg
NM_007298.3:c.787+161C>G	NP_009229.2:n.787+161C>G
NM_007299.3:c.787+161C>G	NP_009230.2:n.787+161C>G
NM_007300.3:c.948C>G	NP_009231.2:p.Ser316Arg
NR_027676.1:n.1084C>G
NM_007294.4:c.948C>G MANE Select	NP_009225.1:p.Ser316Arg
NM_007297.4:c.807C>G	NP_009228.2:p.Ser269Arg
NM_007299.4:c.787+161C>G	NP_009230.2:n.787+161C>G
NM_007300.4:c.948C>G	NP_009231.2:p.Ser316Arg
NR_027676.2:n.1125C>G