Canonical Allele Identifier: CA2260783012

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092517_43092518delinsTC , CM000679.2:g.43092517_43092518delinsTC	GRCh38
NC_000017.10:g.41244534_41244535delinsTC , CM000679.1:g.41244534_41244535delinsTC	GRCh37
NC_000017.9:g.38498060_38498061delinsTC	NCBI36
NG_005905.2:g.125466_125467delinsGA , LRG_292:g.125466_125467delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.3077_3078delinsGA
ENST00000461574.2:c.3013_3014delinsGA	ENSP00000417241.2:p.Glu1005=
ENST00000470026.6:c.3013_3014delinsGA	ENSP00000419274.2:p.Glu1005=
ENST00000473961.6:c.2887_2888delinsGA	ENSP00000420201.2:p.Glu963=
ENST00000476777.6:c.3010_3011delinsGA	ENSP00000417554.2:p.Glu1004=
ENST00000477152.6:c.2935_2936delinsGA	ENSP00000419988.2:p.Glu979=
ENST00000478531.6:c.785-1486_785-1485delinsGA	ENSP00000420412.2:n.785-1486_785-1485delinsGA
ENST00000489037.2:c.2935_2936delinsGA	ENSP00000420781.2:p.Glu979=
ENST00000493919.6:c.647-1486_647-1485delinsGA	ENSP00000418819.2:n.647-1486_647-1485delinsGA
ENST00000494123.6:c.3013_3014delinsGA	ENSP00000419103.2:p.Glu1005=
ENST00000497488.2:c.2125_2126delinsGA	ENSP00000418986.2:p.Glu709=
ENST00000618469.2:c.3013_3014delinsGA	ENSP00000478114.2:p.Glu1005=
ENST00000634433.2:c.2890_2891delinsGA	ENSP00000489431.2:p.Glu964=
ENST00000644379.2:c.3013_3014delinsGA	ENSP00000496570.2:p.Glu1005=
ENST00000644555.2:c.647-1486_647-1485delinsGA	ENSP00000494614.2:n.647-1486_647-1485delinsGA
ENST00000652672.2:c.2872_2873delinsGA	ENSP00000498906.2:p.Glu958=
ENST00000484087.6:c.665-1486_665-1485delinsGA	ENSP00000419481.2:n.665-1486_665-1485delinsGA
ENST00000700182.1:c.707-1486_707-1485delinsGA	ENSP00000514849.1:n.707-1486_707-1485delinsGA
ENST00000357654.9:c.3013_3014delinsGA MANE Select	ENSP00000350283.3:p.Glu1005=
ENST00000471181.7:c.3013_3014delinsGA	ENSP00000418960.2:p.Glu1005=
ENST00000352993.7:c.671-1486_671-1485delinsGA	ENSP00000312236.5:n.671-1486_671-1485delinsGA
ENST00000354071.7:c.3013_3014delinsGA	ENSP00000326002.7:p.Glu1005=
ENST00000357654.7:c.3013_3014delinsGA	ENSP00000350283.3:p.Glu1005=
ENST00000461221.5:c.*2796_*2797delinsGA	ENSP00000418548.1:n.*2796_*2797delinsGA
ENST00000468300.5:c.788-1486_788-1485delinsGA	ENSP00000417148.1:n.788-1486_788-1485delinsGA
ENST00000471181.6:c.3013_3014delinsGA	ENSP00000418960.2:p.Glu1005=
ENST00000478531.5:c.785-1486_785-1485delinsGA	ENSP00000420412.1:n.785-1486_785-1485delinsGA
ENST00000484087.5:c.410-1486_410-1485delinsGA	ENSP00000419481.1:n.410-1486_410-1485delinsGA
ENST00000487825.5:c.413-1486_413-1485delinsGA	ENSP00000418212.1:n.413-1486_413-1485delinsGA
ENST00000491747.6:c.788-1486_788-1485delinsGA	ENSP00000420705.2:n.788-1486_788-1485delinsGA
ENST00000493795.5:c.2872_2873delinsGA	ENSP00000418775.1:p.Glu958=
ENST00000493919.5:c.647-1486_647-1485delinsGA	ENSP00000418819.1:n.647-1486_647-1485delinsGA
ENST00000586385.5:c.5-28567_5-28566delinsGA	ENSP00000465818.1:n.5-28567_5-28566delinsGA
ENST00000591534.5:c.-43-17997_-43-17996delinsGA	ENSP00000467329.1:n.-43-17997_-43-17996delinsGA
ENST00000591849.5:c.-99+32753_-99+32754delinsGA	ENSP00000465347.1:n.-99+32753_-99+32754delinsGA
NM_007294.3:c.3013_3014delinsGA , LRG_292t1:c.3013_3014delinsGA	NP_009225.1:p.Glu1005=
NM_007297.3:c.2872_2873delinsGA	NP_009228.2:p.Glu958=
NM_007298.3:c.788-1486_788-1485delinsGA	NP_009229.2:n.788-1486_788-1485delinsGA
NM_007299.3:c.788-1486_788-1485delinsGA	NP_009230.2:n.788-1486_788-1485delinsGA
NM_007300.3:c.3013_3014delinsGA	NP_009231.2:p.Glu1005=
NR_027676.1:n.3149_3150delinsGA
NM_007294.4:c.3013_3014delinsGA MANE Select	NP_009225.1:p.Glu1005=
NM_007297.4:c.2872_2873delinsGA	NP_009228.2:p.Glu958=
NM_007299.4:c.788-1486_788-1485delinsGA	NP_009230.2:n.788-1486_788-1485delinsGA
NM_007300.4:c.3013_3014delinsGA	NP_009231.2:p.Glu1005=
NR_027676.2:n.3190_3191delinsGA