Canonical Allele Identifier: CA10589959

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 266145
• ClinVar RCV Id: RCV000257820
• dbSNP Id: rs886039934
• MyVariant Identifiers: chr17:g.41246337_41246338insAG (hg19) ; chr17:g.43094320_43094321insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094320_43094321insAG , CM000679.2:g.43094320_43094321insAG	GRCh38
NC_000017.10:g.41246337_41246338insAG , CM000679.1:g.41246337_41246338insAG	GRCh37
NC_000017.9:g.38499863_38499864insAG	NCBI36
NG_005905.2:g.123663_123664insCT , LRG_292:g.123663_123664insCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.1274_1275insCT
ENST00000461574.2:c.1210_1211insCT	ENSP00000417241.2:p.Glu404AlafsTer7
ENST00000470026.6:c.1210_1211insCT	ENSP00000419274.2:p.Glu404AlafsTer7
ENST00000473961.6:c.1084_1085insCT	ENSP00000420201.2:p.Glu362AlafsTer7
ENST00000476777.6:c.1207_1208insCT	ENSP00000417554.2:p.Glu403AlafsTer7
ENST00000477152.6:c.1132_1133insCT	ENSP00000419988.2:p.Glu378AlafsTer7
ENST00000478531.6:c.784+423_784+424insCT	ENSP00000420412.2:n.784+423_784+424insCT
ENST00000489037.2:c.1132_1133insCT	ENSP00000420781.2:p.Glu378AlafsTer7
ENST00000493919.6:c.646+423_646+424insCT	ENSP00000418819.2:n.646+423_646+424insCT
ENST00000494123.6:c.1210_1211insCT	ENSP00000419103.2:p.Glu404AlafsTer7
ENST00000497488.2:c.322_323insCT	ENSP00000418986.2:p.Glu108AlafsTer7
ENST00000618469.2:c.1210_1211insCT	ENSP00000478114.2:p.Glu404AlafsTer7
ENST00000634433.2:c.1087_1088insCT	ENSP00000489431.2:p.Glu363AlafsTer7
ENST00000644379.2:c.1210_1211insCT	ENSP00000496570.2:p.Glu404AlafsTer7
ENST00000644555.2:c.646+423_646+424insCT	ENSP00000494614.2:n.646+423_646+424insCT
ENST00000652672.2:c.1069_1070insCT	ENSP00000498906.2:p.Glu357AlafsTer7
ENST00000484087.6:c.664+423_664+424insCT	ENSP00000419481.2:n.664+423_664+424insCT
ENST00000700182.1:c.706+423_706+424insCT	ENSP00000514849.1:n.706+423_706+424insCT
ENST00000700183.1:c.*1218_*1219insCT	ENSP00000514850.1:n.*1218_*1219insCT
ENST00000357654.9:c.1210_1211insCT MANE Select	ENSP00000350283.3:p.Glu404AlafsTer7
ENST00000471181.7:c.1210_1211insCT	ENSP00000418960.2:p.Glu404AlafsTer7
ENST00000652672.1:c.1069_1070insCT	ENSP00000498906.1:p.Glu357AlafsTer7
ENST00000352993.7:c.670+1525_670+1526insCT	ENSP00000312236.5:n.670+1525_670+1526insC...
ENST00000354071.7:c.1210_1211insCT	ENSP00000326002.7:p.Glu404AlafsTer7
ENST00000357654.7:c.1210_1211insCT	ENSP00000350283.3:p.Glu404AlafsTer7
ENST00000412061.3:c.561_562insCT
ENST00000461221.5:c.*993_*994insCT	ENSP00000418548.1:n.*993_*994insCT
ENST00000468300.5:c.787+423_787+424insCT	ENSP00000417148.1:n.787+423_787+424insCT
ENST00000470026.5:c.1210_1211insCT	ENSP00000419274.1:p.Glu404AlafsTer7
ENST00000471181.6:c.1210_1211insCT	ENSP00000418960.2:p.Glu404AlafsTer7
ENST00000473961.5:c.807_808insCT
ENST00000477152.5:c.1132_1133insCT	ENSP00000419988.1:p.Glu378AlafsTer7
ENST00000478531.5:c.784+423_784+424insCT	ENSP00000420412.1:n.784+423_784+424insCT
ENST00000484087.5:c.409+423_409+424insCT	ENSP00000419481.1:n.409+423_409+424insCT
ENST00000487825.5:c.412+423_412+424insCT	ENSP00000418212.1:n.412+423_412+424insCT
ENST00000491747.6:c.787+423_787+424insCT	ENSP00000420705.2:n.787+423_787+424insCT
ENST00000492859.5:c.*1146_*1147insCT	ENSP00000420253.1:n.*1146_*1147insCT
ENST00000493795.5:c.1069_1070insCT	ENSP00000418775.1:p.Glu357AlafsTer7
ENST00000493919.5:c.646+423_646+424insCT	ENSP00000418819.1:n.646+423_646+424insCT
ENST00000494123.5:c.1210_1211insCT	ENSP00000419103.1:p.Glu404AlafsTer7
ENST00000497488.1:c.322_323insCT	ENSP00000418986.1:p.Glu108AlafsTer7
ENST00000586385.5:c.5-30370_5-30369insCT	ENSP00000465818.1:n.5-30370_5-30369insCT
ENST00000591534.5:c.-43-19800_-43-19799insCT	ENSP00000467329.1:n.-43-19800_-43-19799in...
ENST00000591849.5:c.-99+30950_-99+30951insCT	ENSP00000465347.1:n.-99+30950_-99+30951in...
ENST00000634433.1:c.1087_1088insCT	ENSP00000489431.1:p.Glu363AlafsTer7
NM_007294.3:c.1210_1211insCT , LRG_292t1:c.1210_1211insCT	NP_009225.1:p.Glu404AlafsTer7
NM_007297.3:c.1069_1070insCT	NP_009228.2:p.Glu357AlafsTer7
NM_007298.3:c.787+423_787+424insCT	NP_009229.2:n.787+423_787+424insCT
NM_007299.3:c.787+423_787+424insCT	NP_009230.2:n.787+423_787+424insCT
NM_007300.3:c.1210_1211insCT	NP_009231.2:p.Glu404AlafsTer7
NR_027676.1:n.1346_1347insCT
NM_007294.4:c.1210_1211insCT MANE Select	NP_009225.1:p.Glu404AlafsTer7
NM_007297.4:c.1069_1070insCT	NP_009228.2:p.Glu357AlafsTer7
NM_007299.4:c.787+423_787+424insCT	NP_009230.2:n.787+423_787+424insCT
NM_007300.4:c.1210_1211insCT	NP_009231.2:p.Glu404AlafsTer7
NR_027676.2:n.1387_1388insCT