Canonical Allele Identifier: CA2260782069

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091582_43091583delinsAG , CM000679.2:g.43091582_43091583delinsAG	GRCh38
NC_000017.10:g.41243599_41243600delinsAG , CM000679.1:g.41243599_41243600delinsAG	GRCh37
NC_000017.9:g.38497125_38497126delinsAG	NCBI36
NG_005905.2:g.126401_126402delinsCT , LRG_292:g.126401_126402delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.4012_4013delinsCT
ENST00000461574.2:c.3948_3949delinsCT	ENSP00000417241.2:p.Phe1316=
ENST00000470026.6:c.3948_3949delinsCT	ENSP00000419274.2:p.Phe1316=
ENST00000473961.6:c.3822_3823delinsCT	ENSP00000420201.2:p.Phe1274=
ENST00000476777.6:c.3945_3946delinsCT	ENSP00000417554.2:p.Phe1315=
ENST00000477152.6:c.3870_3871delinsCT	ENSP00000419988.2:p.Phe1290=
ENST00000478531.6:c.785-551_785-550delinsCT	ENSP00000420412.2:n.785-551_785-550delinsCT
ENST00000489037.2:c.3870_3871delinsCT	ENSP00000420781.2:p.Phe1290=
ENST00000493919.6:c.647-551_647-550delinsCT	ENSP00000418819.2:n.647-551_647-550delinsCT
ENST00000494123.6:c.3948_3949delinsCT	ENSP00000419103.2:p.Phe1316=
ENST00000497488.2:c.3060_3061delinsCT	ENSP00000418986.2:p.Phe1020=
ENST00000618469.2:c.3948_3949delinsCT	ENSP00000478114.2:p.Phe1316=
ENST00000634433.2:c.3825_3826delinsCT	ENSP00000489431.2:p.Phe1275=
ENST00000644379.2:c.3948_3949delinsCT	ENSP00000496570.2:p.Phe1316=
ENST00000644555.2:c.647-551_647-550delinsCT	ENSP00000494614.2:n.647-551_647-550delinsCT
ENST00000652672.2:c.3807_3808delinsCT	ENSP00000498906.2:p.Phe1269=
ENST00000484087.6:c.665-551_665-550delinsCT	ENSP00000419481.2:n.665-551_665-550delinsCT
ENST00000700182.1:c.707-551_707-550delinsCT	ENSP00000514849.1:n.707-551_707-550delinsCT
ENST00000357654.9:c.3948_3949delinsCT MANE Select	ENSP00000350283.3:p.Phe1316=
ENST00000471181.7:c.3948_3949delinsCT	ENSP00000418960.2:p.Phe1316=
ENST00000644379.1:c.269_270delinsCT
ENST00000352993.7:c.671-551_671-550delinsCT	ENSP00000312236.5:n.671-551_671-550delinsCT
ENST00000354071.7:c.3948_3949delinsCT	ENSP00000326002.7:p.Phe1316=
ENST00000357654.7:c.3948_3949delinsCT	ENSP00000350283.3:p.Phe1316=
ENST00000461221.5:c.*3731_*3732delinsCT	ENSP00000418548.1:n.*3731_*3732delinsCT
ENST00000461574.1:c.242_243delinsCT
ENST00000468300.5:c.788-551_788-550delinsCT	ENSP00000417148.1:n.788-551_788-550delinsCT
ENST00000471181.6:c.3948_3949delinsCT	ENSP00000418960.2:p.Phe1316=
ENST00000478531.5:c.785-551_785-550delinsCT	ENSP00000420412.1:n.785-551_785-550delinsCT
ENST00000484087.5:c.410-551_410-550delinsCT	ENSP00000419481.1:n.410-551_410-550delinsCT
ENST00000487825.5:c.413-551_413-550delinsCT	ENSP00000418212.1:n.413-551_413-550delinsCT
ENST00000491747.6:c.788-551_788-550delinsCT	ENSP00000420705.2:n.788-551_788-550delinsCT
ENST00000493795.5:c.3807_3808delinsCT	ENSP00000418775.1:p.Phe1269=
ENST00000493919.5:c.647-551_647-550delinsCT	ENSP00000418819.1:n.647-551_647-550delinsCT
ENST00000586385.5:c.5-27632_5-27631delinsCT	ENSP00000465818.1:n.5-27632_5-27631delinsCT
ENST00000591534.5:c.-43-17062_-43-17061delinsCT	ENSP00000467329.1:n.-43-17062_-43-17061delinsCT
ENST00000591849.5:c.-99+33688_-99+33689delinsCT	ENSP00000465347.1:n.-99+33688_-99+33689delinsCT
NM_007294.3:c.3948_3949delinsCT , LRG_292t1:c.3948_3949delinsCT	NP_009225.1:p.Phe1316=
NM_007297.3:c.3807_3808delinsCT	NP_009228.2:p.Phe1269=
NM_007298.3:c.788-551_788-550delinsCT	NP_009229.2:n.788-551_788-550delinsCT
NM_007299.3:c.788-551_788-550delinsCT	NP_009230.2:n.788-551_788-550delinsCT
NM_007300.3:c.3948_3949delinsCT	NP_009231.2:p.Phe1316=
NR_027676.1:n.4084_4085delinsCT
NM_007294.4:c.3948_3949delinsCT MANE Select	NP_009225.1:p.Phe1316=
NM_007297.4:c.3807_3808delinsCT	NP_009228.2:p.Phe1269=
NM_007299.4:c.788-551_788-550delinsCT	NP_009230.2:n.788-551_788-550delinsCT
NM_007300.4:c.3948_3949delinsCT	NP_009231.2:p.Phe1316=
NR_027676.2:n.4125_4126delinsCT