Canonical Allele Identifier: CA003878

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 55706
• ClinVar RCV Id: RCV000112787 ; RCV003157388 ; RCV001853031
• dbSNP Id: rs80357214
• MyVariant Identifiers: chr17:g.41246756A>C (hg19) ; chr17:g.43094739A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094739A>C , CM000679.2:g.43094739A>C	GRCh38
NC_000017.10:g.41246756A>C , CM000679.1:g.41246756A>C	GRCh37
NC_000017.9:g.38500282A>C	NCBI36
NG_005905.2:g.123245T>G , LRG_292:g.123245T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.856T>G
ENST00000461574.2:c.792T>G	ENSP00000417241.2:p.Ser264Arg
ENST00000470026.6:c.792T>G	ENSP00000419274.2:p.Ser264Arg
ENST00000473961.6:c.666T>G	ENSP00000420201.2:p.Ser222Arg
ENST00000476777.6:c.789T>G	ENSP00000417554.2:p.Ser263Arg
ENST00000477152.6:c.714T>G	ENSP00000419988.2:p.Ser238Arg
ENST00000478531.6:c.784+5T>G	ENSP00000420412.2:n.784+5T>G
ENST00000489037.2:c.714T>G	ENSP00000420781.2:p.Ser238Arg
ENST00000493919.6:c.646+5T>G	ENSP00000418819.2:n.646+5T>G
ENST00000494123.6:c.792T>G	ENSP00000419103.2:p.Ser264Arg
ENST00000497488.2:c.-97T>G	ENSP00000418986.2:n.-97T>G
ENST00000618469.2:c.792T>G	ENSP00000478114.2:p.Ser264Arg
ENST00000634433.2:c.669T>G	ENSP00000489431.2:p.Ser223Arg
ENST00000644379.2:c.792T>G	ENSP00000496570.2:p.Ser264Arg
ENST00000644555.2:c.646+5T>G	ENSP00000494614.2:n.646+5T>G
ENST00000652672.2:c.651T>G	ENSP00000498906.2:p.Ser217Arg
ENST00000484087.6:c.664+5T>G	ENSP00000419481.2:n.664+5T>G
ENST00000700182.1:c.706+5T>G	ENSP00000514849.1:n.706+5T>G
ENST00000700183.1:c.*800T>G	ENSP00000514850.1:n.*800T>G
ENST00000357654.9:c.792T>G MANE Select	ENSP00000350283.3:p.Ser264Arg
ENST00000471181.7:c.792T>G	ENSP00000418960.2:p.Ser264Arg
ENST00000642945.1:c.*666T>G	ENSP00000495897.1:n.*666T>G
ENST00000652672.1:c.651T>G	ENSP00000498906.1:p.Ser217Arg
ENST00000352993.7:c.670+1107T>G	ENSP00000312236.5:n.670+1107T>G
ENST00000354071.7:c.792T>G	ENSP00000326002.7:p.Ser264Arg
ENST00000357654.7:c.792T>G	ENSP00000350283.3:p.Ser264Arg
ENST00000412061.3:c.143T>G
ENST00000461221.5:c.*575T>G	ENSP00000418548.1:n.*575T>G
ENST00000468300.5:c.787+5T>G	ENSP00000417148.1:n.787+5T>G
ENST00000470026.5:c.792T>G	ENSP00000419274.1:p.Ser264Arg
ENST00000471181.6:c.792T>G	ENSP00000418960.2:p.Ser264Arg
ENST00000473961.5:c.389T>G
ENST00000477152.5:c.714T>G	ENSP00000419988.1:p.Ser238Arg
ENST00000478531.5:c.784+5T>G	ENSP00000420412.1:n.784+5T>G
ENST00000484087.5:c.409+5T>G	ENSP00000419481.1:n.409+5T>G
ENST00000487825.5:c.412+5T>G	ENSP00000418212.1:n.412+5T>G
ENST00000491747.6:c.787+5T>G	ENSP00000420705.2:n.787+5T>G
ENST00000492859.5:c.*728T>G	ENSP00000420253.1:n.*728T>G
ENST00000493795.5:c.651T>G	ENSP00000418775.1:p.Ser217Arg
ENST00000493919.5:c.646+5T>G	ENSP00000418819.1:n.646+5T>G
ENST00000494123.5:c.792T>G	ENSP00000419103.1:p.Ser264Arg
ENST00000497488.1:c.-97T>G	ENSP00000418986.1:n.-97T>G
ENST00000586385.5:c.4+30443T>G	ENSP00000465818.1:n.4+30443T>G
ENST00000591534.5:c.-43-20218T>G	ENSP00000467329.1:n.-43-20218T>G
ENST00000591849.5:c.-99+30532T>G	ENSP00000465347.1:n.-99+30532T>G
ENST00000634433.1:c.669T>G	ENSP00000489431.1:p.Ser223Arg
NM_007294.3:c.792T>G , LRG_292t1:c.792T>G	NP_009225.1:p.Ser264Arg
NM_007297.3:c.651T>G	NP_009228.2:p.Ser217Arg
NM_007298.3:c.787+5T>G	NP_009229.2:n.787+5T>G
NM_007299.3:c.787+5T>G	NP_009230.2:n.787+5T>G
NM_007300.3:c.792T>G	NP_009231.2:p.Ser264Arg
NR_027676.1:n.928T>G
NM_007294.4:c.792T>G MANE Select	NP_009225.1:p.Ser264Arg
NM_007297.4:c.651T>G	NP_009228.2:p.Ser217Arg
NM_007299.4:c.787+5T>G	NP_009230.2:n.787+5T>G
NM_007300.4:c.792T>G	NP_009231.2:p.Ser264Arg
NR_027676.2:n.969T>G