Canonical Allele Identifier: CA10600231

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 482907
• ClinVar RCV Id: RCV000572449 ; RCV000691850 ; RCV000758853
• dbSNP Id: rs1216516227
• gnomAD v2: 17-41246629-T-C
• MyVariant Identifiers: chr17:g.41246629T>C (hg19) ; chr17:g.43094612T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094612T>C , CM000679.2:g.43094612T>C	GRCh38
NC_000017.10:g.41246629T>C , CM000679.1:g.41246629T>C	GRCh37
NC_000017.9:g.38500155T>C	NCBI36
NG_005905.2:g.123372A>G , LRG_292:g.123372A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.983A>G
ENST00000461574.2:c.919A>G	ENSP00000417241.2:p.Lys307Glu
ENST00000470026.6:c.919A>G	ENSP00000419274.2:p.Lys307Glu
ENST00000473961.6:c.793A>G	ENSP00000420201.2:p.Lys265Glu
ENST00000476777.6:c.916A>G	ENSP00000417554.2:p.Lys306Glu
ENST00000477152.6:c.841A>G	ENSP00000419988.2:p.Lys281Glu
ENST00000478531.6:c.784+132A>G	ENSP00000420412.2:n.784+132A>G
ENST00000489037.2:c.841A>G	ENSP00000420781.2:p.Lys281Glu
ENST00000493919.6:c.646+132A>G	ENSP00000418819.2:n.646+132A>G
ENST00000494123.6:c.919A>G	ENSP00000419103.2:p.Lys307Glu
ENST00000497488.2:c.31A>G	ENSP00000418986.2:p.Lys11Glu
ENST00000618469.2:c.919A>G	ENSP00000478114.2:p.Lys307Glu
ENST00000634433.2:c.796A>G	ENSP00000489431.2:p.Lys266Glu
ENST00000644379.2:c.919A>G	ENSP00000496570.2:p.Lys307Glu
ENST00000644555.2:c.646+132A>G	ENSP00000494614.2:n.646+132A>G
ENST00000652672.2:c.778A>G	ENSP00000498906.2:p.Lys260Glu
ENST00000484087.6:c.664+132A>G	ENSP00000419481.2:n.664+132A>G
ENST00000700182.1:c.706+132A>G	ENSP00000514849.1:n.706+132A>G
ENST00000700183.1:c.*927A>G	ENSP00000514850.1:n.*927A>G
ENST00000357654.9:c.919A>G MANE Select	ENSP00000350283.3:p.Lys307Glu
ENST00000471181.7:c.919A>G	ENSP00000418960.2:p.Lys307Glu
ENST00000642945.1:c.*793A>G	ENSP00000495897.1:n.*793A>G
ENST00000652672.1:c.778A>G	ENSP00000498906.1:p.Lys260Glu
ENST00000352993.7:c.670+1234A>G	ENSP00000312236.5:n.670+1234A>G
ENST00000354071.7:c.919A>G	ENSP00000326002.7:p.Lys307Glu
ENST00000357654.7:c.919A>G	ENSP00000350283.3:p.Lys307Glu
ENST00000412061.3:c.270A>G
ENST00000461221.5:c.*702A>G	ENSP00000418548.1:n.*702A>G
ENST00000468300.5:c.787+132A>G	ENSP00000417148.1:n.787+132A>G
ENST00000470026.5:c.919A>G	ENSP00000419274.1:p.Lys307Glu
ENST00000471181.6:c.919A>G	ENSP00000418960.2:p.Lys307Glu
ENST00000473961.5:c.516A>G
ENST00000477152.5:c.841A>G	ENSP00000419988.1:p.Lys281Glu
ENST00000478531.5:c.784+132A>G	ENSP00000420412.1:n.784+132A>G
ENST00000484087.5:c.409+132A>G	ENSP00000419481.1:n.409+132A>G
ENST00000487825.5:c.412+132A>G	ENSP00000418212.1:n.412+132A>G
ENST00000491747.6:c.787+132A>G	ENSP00000420705.2:n.787+132A>G
ENST00000492859.5:c.*855A>G	ENSP00000420253.1:n.*855A>G
ENST00000493795.5:c.778A>G	ENSP00000418775.1:p.Lys260Glu
ENST00000493919.5:c.646+132A>G	ENSP00000418819.1:n.646+132A>G
ENST00000494123.5:c.919A>G	ENSP00000419103.1:p.Lys307Glu
ENST00000497488.1:c.31A>G	ENSP00000418986.1:p.Lys11Glu
ENST00000586385.5:c.4+30570A>G	ENSP00000465818.1:n.4+30570A>G
ENST00000591534.5:c.-43-20091A>G	ENSP00000467329.1:n.-43-20091A>G
ENST00000591849.5:c.-99+30659A>G	ENSP00000465347.1:n.-99+30659A>G
ENST00000634433.1:c.796A>G	ENSP00000489431.1:p.Lys266Glu
NM_007294.3:c.919A>G , LRG_292t1:c.919A>G	NP_009225.1:p.Lys307Glu
NM_007297.3:c.778A>G	NP_009228.2:p.Lys260Glu
NM_007298.3:c.787+132A>G	NP_009229.2:n.787+132A>G
NM_007299.3:c.787+132A>G	NP_009230.2:n.787+132A>G
NM_007300.3:c.919A>G	NP_009231.2:p.Lys307Glu
NR_027676.1:n.1055A>G
NM_007294.4:c.919A>G MANE Select	NP_009225.1:p.Lys307Glu
NM_007297.4:c.778A>G	NP_009228.2:p.Lys260Glu
NM_007299.4:c.787+132A>G	NP_009230.2:n.787+132A>G
NM_007300.4:c.919A>G	NP_009231.2:p.Lys307Glu
NR_027676.2:n.1096A>G