Canonical Allele Identifier: CA2963271657

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091584_43091585insGAA , CM000679.2:g.43091584_43091585insGAA	GRCh38
NC_000017.10:g.41243601_41243602insGAA , CM000679.1:g.41243601_41243602insGAA	GRCh37
NC_000017.9:g.38497127_38497128insGAA	NCBI36
NG_005905.2:g.126400_126401insTCT , LRG_292:g.126400_126401insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.4011_4012insTCT
ENST00000461574.2:c.3947_3948insTCT	ENSP00000417241.2:p.Phe1316_Leu1317insLeu
ENST00000470026.6:c.3947_3948insTCT	ENSP00000419274.2:p.Phe1316_Leu1317insLeu
ENST00000473961.6:c.3821_3822insTCT	ENSP00000420201.2:p.Phe1274_Leu1275insLeu
ENST00000476777.6:c.3944_3945insTCT	ENSP00000417554.2:p.Phe1315_Leu1316insLeu
ENST00000477152.6:c.3869_3870insTCT	ENSP00000419988.2:p.Phe1290_Leu1291insLeu
ENST00000478531.6:c.785-552_785-551insTCT	ENSP00000420412.2:n.785-552_785-551insTCT
ENST00000489037.2:c.3869_3870insTCT	ENSP00000420781.2:p.Phe1290_Leu1291insLeu
ENST00000493919.6:c.647-552_647-551insTCT	ENSP00000418819.2:n.647-552_647-551insTCT
ENST00000494123.6:c.3947_3948insTCT	ENSP00000419103.2:p.Phe1316_Leu1317insLeu
ENST00000497488.2:c.3059_3060insTCT	ENSP00000418986.2:p.Phe1020_Leu1021insLeu
ENST00000618469.2:c.3947_3948insTCT	ENSP00000478114.2:p.Phe1316_Leu1317insLeu
ENST00000634433.2:c.3824_3825insTCT	ENSP00000489431.2:p.Phe1275_Leu1276insLeu
ENST00000644379.2:c.3947_3948insTCT	ENSP00000496570.2:p.Phe1316_Leu1317insLeu
ENST00000644555.2:c.647-552_647-551insTCT	ENSP00000494614.2:n.647-552_647-551insTCT
ENST00000652672.2:c.3806_3807insTCT	ENSP00000498906.2:p.Phe1269_Leu1270insLeu
ENST00000484087.6:c.665-552_665-551insTCT	ENSP00000419481.2:n.665-552_665-551insTCT
ENST00000700182.1:c.707-552_707-551insTCT	ENSP00000514849.1:n.707-552_707-551insTCT
ENST00000357654.9:c.3947_3948insTCT MANE Select	ENSP00000350283.3:p.Phe1316_Leu1317insLeu
ENST00000471181.7:c.3947_3948insTCT	ENSP00000418960.2:p.Phe1316_Leu1317insLeu
ENST00000644379.1:c.268_269insTCT
ENST00000352993.7:c.671-552_671-551insTCT	ENSP00000312236.5:n.671-552_671-551insTCT
ENST00000354071.7:c.3947_3948insTCT	ENSP00000326002.7:p.Phe1316_Leu1317insLeu
ENST00000357654.7:c.3947_3948insTCT	ENSP00000350283.3:p.Phe1316_Leu1317insLeu
ENST00000461221.5:c.*3730_*3731insTCT	ENSP00000418548.1:n.*3730_*3731insTCT
ENST00000461574.1:c.241_242insTCT
ENST00000468300.5:c.788-552_788-551insTCT	ENSP00000417148.1:n.788-552_788-551insTCT
ENST00000471181.6:c.3947_3948insTCT	ENSP00000418960.2:p.Phe1316_Leu1317insLeu
ENST00000478531.5:c.785-552_785-551insTCT	ENSP00000420412.1:n.785-552_785-551insTCT
ENST00000484087.5:c.410-552_410-551insTCT	ENSP00000419481.1:n.410-552_410-551insTCT
ENST00000487825.5:c.413-552_413-551insTCT	ENSP00000418212.1:n.413-552_413-551insTCT
ENST00000491747.6:c.788-552_788-551insTCT	ENSP00000420705.2:n.788-552_788-551insTCT
ENST00000493795.5:c.3806_3807insTCT	ENSP00000418775.1:p.Phe1269_Leu1270insLeu
ENST00000493919.5:c.647-552_647-551insTCT	ENSP00000418819.1:n.647-552_647-551insTCT
ENST00000586385.5:c.5-27633_5-27632insTCT	ENSP00000465818.1:n.5-27633_5-27632insTCT
ENST00000591534.5:c.-43-17063_-43-17062insTCT	ENSP00000467329.1:n.-43-17063_-43-17062insTCT
ENST00000591849.5:c.-99+33687_-99+33688insTCT	ENSP00000465347.1:n.-99+33687_-99+33688insTCT
NM_007294.3:c.3947_3948insTCT , LRG_292t1:c.3947_3948insTCT	NP_009225.1:p.Phe1316_Leu1317insLeu
NM_007297.3:c.3806_3807insTCT	NP_009228.2:p.Phe1269_Leu1270insLeu
NM_007298.3:c.788-552_788-551insTCT	NP_009229.2:n.788-552_788-551insTCT
NM_007299.3:c.788-552_788-551insTCT	NP_009230.2:n.788-552_788-551insTCT
NM_007300.3:c.3947_3948insTCT	NP_009231.2:p.Phe1316_Leu1317insLeu
NR_027676.1:n.4083_4084insTCT
NM_007294.4:c.3947_3948insTCT MANE Select	NP_009225.1:p.Phe1316_Leu1317insLeu
NM_007297.4:c.3806_3807insTCT	NP_009228.2:p.Phe1269_Leu1270insLeu
NM_007299.4:c.788-552_788-551insTCT	NP_009230.2:n.788-552_788-551insTCT
NM_007300.4:c.3947_3948insTCT	NP_009231.2:p.Phe1316_Leu1317insLeu
NR_027676.2:n.4124_4125insTCT