Canonical Allele Identifier: CA10598513

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 1444310
• ClinVar RCV Id: RCV001955872 ; RCV002282663 ; RCV002397990
• dbSNP Id: rs1064795270
• MyVariant Identifiers: chr17:g.41245791G>A (hg19) ; chr17:g.43093774G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093774G>A , CM000679.2:g.43093774G>A	GRCh38
NC_000017.10:g.41245791G>A , CM000679.1:g.41245791G>A	GRCh37
NC_000017.9:g.38499317G>A	NCBI36
NG_005905.2:g.124210C>T , LRG_292:g.124210C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1821C>T
ENST00000461574.2:c.1757C>T	ENSP00000417241.2:p.Pro586Leu
ENST00000470026.6:c.1757C>T	ENSP00000419274.2:p.Pro586Leu
ENST00000473961.6:c.1631C>T	ENSP00000420201.2:p.Pro544Leu
ENST00000476777.6:c.1754C>T	ENSP00000417554.2:p.Pro585Leu
ENST00000477152.6:c.1679C>T	ENSP00000419988.2:p.Pro560Leu
ENST00000478531.6:c.784+970C>T	ENSP00000420412.2:n.784+970C>T
ENST00000489037.2:c.1679C>T	ENSP00000420781.2:p.Pro560Leu
ENST00000493919.6:c.646+970C>T	ENSP00000418819.2:n.646+970C>T
ENST00000494123.6:c.1757C>T	ENSP00000419103.2:p.Pro586Leu
ENST00000497488.2:c.869C>T	ENSP00000418986.2:p.Pro290Leu
ENST00000618469.2:c.1757C>T	ENSP00000478114.2:p.Pro586Leu
ENST00000634433.2:c.1634C>T	ENSP00000489431.2:p.Pro545Leu
ENST00000644379.2:c.1757C>T	ENSP00000496570.2:p.Pro586Leu
ENST00000644555.2:c.646+970C>T	ENSP00000494614.2:n.646+970C>T
ENST00000652672.2:c.1616C>T	ENSP00000498906.2:p.Pro539Leu
ENST00000484087.6:c.664+970C>T	ENSP00000419481.2:n.664+970C>T
ENST00000700182.1:c.706+970C>T	ENSP00000514849.1:n.706+970C>T
ENST00000357654.9:c.1757C>T MANE Select	ENSP00000350283.3:p.Pro586Leu
ENST00000471181.7:c.1757C>T	ENSP00000418960.2:p.Pro586Leu
ENST00000652672.1:c.1616C>T	ENSP00000498906.1:p.Pro539Leu
ENST00000352993.7:c.670+2072C>T	ENSP00000312236.5:n.670+2072C>T
ENST00000354071.7:c.1757C>T	ENSP00000326002.7:p.Pro586Leu
ENST00000357654.7:c.1757C>T	ENSP00000350283.3:p.Pro586Leu
ENST00000412061.3:c.1108C>T
ENST00000461221.5:c.*1540C>T	ENSP00000418548.1:n.*1540C>T
ENST00000468300.5:c.787+970C>T	ENSP00000417148.1:n.787+970C>T
ENST00000470026.5:c.1757C>T	ENSP00000419274.1:p.Pro586Leu
ENST00000471181.6:c.1757C>T	ENSP00000418960.2:p.Pro586Leu
ENST00000477152.5:c.1679C>T	ENSP00000419988.1:p.Pro560Leu
ENST00000478531.5:c.784+970C>T	ENSP00000420412.1:n.784+970C>T
ENST00000484087.5:c.409+970C>T	ENSP00000419481.1:n.409+970C>T
ENST00000487825.5:c.412+970C>T	ENSP00000418212.1:n.412+970C>T
ENST00000491747.6:c.787+970C>T	ENSP00000420705.2:n.787+970C>T
ENST00000493795.5:c.1616C>T	ENSP00000418775.1:p.Pro539Leu
ENST00000493919.5:c.646+970C>T	ENSP00000418819.1:n.646+970C>T
ENST00000586385.5:c.5-29823C>T	ENSP00000465818.1:n.5-29823C>T
ENST00000591534.5:c.-43-19253C>T	ENSP00000467329.1:n.-43-19253C>T
ENST00000591849.5:c.-99+31497C>T	ENSP00000465347.1:n.-99+31497C>T
ENST00000634433.1:c.1634C>T	ENSP00000489431.1:p.Pro545Leu
NM_007294.3:c.1757C>T , LRG_292t1:c.1757C>T	NP_009225.1:p.Pro586Leu
NM_007297.3:c.1616C>T	NP_009228.2:p.Pro539Leu
NM_007298.3:c.787+970C>T	NP_009229.2:n.787+970C>T
NM_007299.3:c.787+970C>T	NP_009230.2:n.787+970C>T
NM_007300.3:c.1757C>T	NP_009231.2:p.Pro586Leu
NR_027676.1:n.1893C>T
NM_007294.4:c.1757C>T MANE Select	NP_009225.1:p.Pro586Leu
NM_007297.4:c.1616C>T	NP_009228.2:p.Pro539Leu
NM_007299.4:c.787+970C>T	NP_009230.2:n.787+970C>T
NM_007300.4:c.1757C>T	NP_009231.2:p.Pro586Leu
NR_027676.2:n.1934C>T