Canonical Allele Identifier: CA000866

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 91545
• ClinVar RCV Id: RCV000077062 ; RCV000413037 ; RCV000709489 ; RCV002381393
• dbSNP Id: rs398122630
• MyVariant Identifiers: chr17:g.41246221T>A (hg19) ; chr17:g.43094204T>A (hg38)
• PubMed: PMID:23469205 ; PMID:24884479

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094204T>A , CM000679.2:g.43094204T>A	GRCh38
NC_000017.10:g.41246221T>A , CM000679.1:g.41246221T>A	GRCh37
NC_000017.9:g.38499747T>A	NCBI36
NG_005905.2:g.123780A>T , LRG_292:g.123780A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1391A>T
ENST00000461574.2:c.1327A>T	ENSP00000417241.2:p.Lys443Ter
ENST00000470026.6:c.1327A>T	ENSP00000419274.2:p.Lys443Ter
ENST00000473961.6:c.1201A>T	ENSP00000420201.2:p.Lys401Ter
ENST00000476777.6:c.1324A>T	ENSP00000417554.2:p.Lys442Ter
ENST00000477152.6:c.1249A>T	ENSP00000419988.2:p.Lys417Ter
ENST00000478531.6:c.784+540A>T	ENSP00000420412.2:n.784+540A>T
ENST00000489037.2:c.1249A>T	ENSP00000420781.2:p.Lys417Ter
ENST00000493919.6:c.646+540A>T	ENSP00000418819.2:n.646+540A>T
ENST00000494123.6:c.1327A>T	ENSP00000419103.2:p.Lys443Ter
ENST00000497488.2:c.439A>T	ENSP00000418986.2:p.Lys147Ter
ENST00000618469.2:c.1327A>T	ENSP00000478114.2:p.Lys443Ter
ENST00000634433.2:c.1204A>T	ENSP00000489431.2:p.Lys402Ter
ENST00000644379.2:c.1327A>T	ENSP00000496570.2:p.Lys443Ter
ENST00000644555.2:c.646+540A>T	ENSP00000494614.2:n.646+540A>T
ENST00000652672.2:c.1186A>T	ENSP00000498906.2:p.Lys396Ter
ENST00000484087.6:c.664+540A>T	ENSP00000419481.2:n.664+540A>T
ENST00000700182.1:c.706+540A>T	ENSP00000514849.1:n.706+540A>T
ENST00000700183.1:c.*1335A>T	ENSP00000514850.1:n.*1335A>T
ENST00000357654.9:c.1327A>T MANE Select	ENSP00000350283.3:p.Lys443Ter
ENST00000471181.7:c.1327A>T	ENSP00000418960.2:p.Lys443Ter
ENST00000652672.1:c.1186A>T	ENSP00000498906.1:p.Lys396Ter
ENST00000352993.7:c.670+1642A>T	ENSP00000312236.5:n.670+1642A>T
ENST00000354071.7:c.1327A>T	ENSP00000326002.7:p.Lys443Ter
ENST00000357654.7:c.1327A>T	ENSP00000350283.3:p.Lys443Ter
ENST00000412061.3:c.678A>T
ENST00000461221.5:c.*1110A>T	ENSP00000418548.1:n.*1110A>T
ENST00000468300.5:c.787+540A>T	ENSP00000417148.1:n.787+540A>T
ENST00000470026.5:c.1327A>T	ENSP00000419274.1:p.Lys443Ter
ENST00000471181.6:c.1327A>T	ENSP00000418960.2:p.Lys443Ter
ENST00000473961.5:c.924A>T
ENST00000477152.5:c.1249A>T	ENSP00000419988.1:p.Lys417Ter
ENST00000478531.5:c.784+540A>T	ENSP00000420412.1:n.784+540A>T
ENST00000484087.5:c.409+540A>T	ENSP00000419481.1:n.409+540A>T
ENST00000487825.5:c.412+540A>T	ENSP00000418212.1:n.412+540A>T
ENST00000491747.6:c.787+540A>T	ENSP00000420705.2:n.787+540A>T
ENST00000492859.5:c.*1263A>T	ENSP00000420253.1:n.*1263A>T
ENST00000493795.5:c.1186A>T	ENSP00000418775.1:p.Lys396Ter
ENST00000493919.5:c.646+540A>T	ENSP00000418819.1:n.646+540A>T
ENST00000494123.5:c.1327A>T	ENSP00000419103.1:p.Lys443Ter
ENST00000497488.1:c.439A>T	ENSP00000418986.1:p.Lys147Ter
ENST00000586385.5:c.5-30253A>T	ENSP00000465818.1:n.5-30253A>T
ENST00000591534.5:c.-43-19683A>T	ENSP00000467329.1:n.-43-19683A>T
ENST00000591849.5:c.-99+31067A>T	ENSP00000465347.1:n.-99+31067A>T
ENST00000634433.1:c.1204A>T	ENSP00000489431.1:p.Lys402Ter
NM_007294.3:c.1327A>T , LRG_292t1:c.1327A>T	NP_009225.1:p.Lys443Ter
NM_007297.3:c.1186A>T	NP_009228.2:p.Lys396Ter
NM_007298.3:c.787+540A>T	NP_009229.2:n.787+540A>T
NM_007299.3:c.787+540A>T	NP_009230.2:n.787+540A>T
NM_007300.3:c.1327A>T	NP_009231.2:p.Lys443Ter
NR_027676.1:n.1463A>T
NM_007294.4:c.1327A>T MANE Select	NP_009225.1:p.Lys443Ter
NM_007297.4:c.1186A>T	NP_009228.2:p.Lys396Ter
NM_007299.4:c.787+540A>T	NP_009230.2:n.787+540A>T
NM_007300.4:c.1327A>T	NP_009231.2:p.Lys443Ter
NR_027676.2:n.1504A>T