Canonical Allele Identifier: CA2260782228

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091749_43091751delinsAAT , CM000679.2:g.43091749_43091751delinsAAT	GRCh38
NC_000017.10:g.41243766_41243768delinsAAT , CM000679.1:g.41243766_41243768delinsAAT	GRCh37
NC_000017.9:g.38497292_38497294delinsAAT	NCBI36
NG_005905.2:g.126233_126235delinsATT , LRG_292:g.126233_126235delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3844_3846delinsATT
ENST00000461574.2:c.3780_3782delinsATT	ENSP00000417241.2:p.Leu1260=
ENST00000470026.6:c.3780_3782delinsATT	ENSP00000419274.2:p.Leu1260=
ENST00000473961.6:c.3654_3656delinsATT	ENSP00000420201.2:p.Leu1218=
ENST00000476777.6:c.3777_3779delinsATT	ENSP00000417554.2:p.Leu1259=
ENST00000477152.6:c.3702_3704delinsATT	ENSP00000419988.2:p.Leu1234=
ENST00000478531.6:c.785-719_785-717delinsATT	ENSP00000420412.2:n.785-719_785-717delinsATT
ENST00000489037.2:c.3702_3704delinsATT	ENSP00000420781.2:p.Leu1234=
ENST00000493919.6:c.647-719_647-717delinsATT	ENSP00000418819.2:n.647-719_647-717delinsATT
ENST00000494123.6:c.3780_3782delinsATT	ENSP00000419103.2:p.Leu1260=
ENST00000497488.2:c.2892_2894delinsATT	ENSP00000418986.2:p.Leu964=
ENST00000618469.2:c.3780_3782delinsATT	ENSP00000478114.2:p.Leu1260=
ENST00000634433.2:c.3657_3659delinsATT	ENSP00000489431.2:p.Leu1219=
ENST00000644379.2:c.3780_3782delinsATT	ENSP00000496570.2:p.Leu1260=
ENST00000644555.2:c.647-719_647-717delinsATT	ENSP00000494614.2:n.647-719_647-717delinsATT
ENST00000652672.2:c.3639_3641delinsATT	ENSP00000498906.2:p.Leu1213=
ENST00000484087.6:c.665-719_665-717delinsATT	ENSP00000419481.2:n.665-719_665-717delinsATT
ENST00000700182.1:c.707-719_707-717delinsATT	ENSP00000514849.1:n.707-719_707-717delinsATT
ENST00000357654.9:c.3780_3782delinsATT MANE Select	ENSP00000350283.3:p.Leu1260=
ENST00000471181.7:c.3780_3782delinsATT	ENSP00000418960.2:p.Leu1260=
ENST00000644379.1:c.101_103delinsATT
ENST00000352993.7:c.671-719_671-717delinsATT	ENSP00000312236.5:n.671-719_671-717delinsATT
ENST00000354071.7:c.3780_3782delinsATT	ENSP00000326002.7:p.Leu1260=
ENST00000357654.7:c.3780_3782delinsATT	ENSP00000350283.3:p.Leu1260=
ENST00000461221.5:c.*3563_*3565delinsATT	ENSP00000418548.1:n.*3563_*3565delinsATT
ENST00000461574.1:c.74_76delinsATT
ENST00000468300.5:c.788-719_788-717delinsATT	ENSP00000417148.1:n.788-719_788-717delinsATT
ENST00000471181.6:c.3780_3782delinsATT	ENSP00000418960.2:p.Leu1260=
ENST00000478531.5:c.785-719_785-717delinsATT	ENSP00000420412.1:n.785-719_785-717delinsATT
ENST00000484087.5:c.410-719_410-717delinsATT	ENSP00000419481.1:n.410-719_410-717delinsATT
ENST00000487825.5:c.413-719_413-717delinsATT	ENSP00000418212.1:n.413-719_413-717delinsATT
ENST00000491747.6:c.788-719_788-717delinsATT	ENSP00000420705.2:n.788-719_788-717delinsATT
ENST00000493795.5:c.3639_3641delinsATT	ENSP00000418775.1:p.Leu1213=
ENST00000493919.5:c.647-719_647-717delinsATT	ENSP00000418819.1:n.647-719_647-717delinsATT
ENST00000586385.5:c.5-27800_5-27798delinsATT	ENSP00000465818.1:n.5-27800_5-27798delinsATT
ENST00000591534.5:c.-43-17230_-43-17228delinsATT	ENSP00000467329.1:n.-43-17230_-43-17228delinsATT
ENST00000591849.5:c.-99+33520_-99+33522delinsATT	ENSP00000465347.1:n.-99+33520_-99+33522delinsATT
NM_007294.3:c.3780_3782delinsATT , LRG_292t1:c.3780_3782delinsATT	NP_009225.1:p.Leu1260=
NM_007297.3:c.3639_3641delinsATT	NP_009228.2:p.Leu1213=
NM_007298.3:c.788-719_788-717delinsATT	NP_009229.2:n.788-719_788-717delinsATT
NM_007299.3:c.788-719_788-717delinsATT	NP_009230.2:n.788-719_788-717delinsATT
NM_007300.3:c.3780_3782delinsATT	NP_009231.2:p.Leu1260=
NR_027676.1:n.3916_3918delinsATT
NM_007294.4:c.3780_3782delinsATT MANE Select	NP_009225.1:p.Leu1260=
NM_007297.4:c.3639_3641delinsATT	NP_009228.2:p.Leu1213=
NM_007299.4:c.788-719_788-717delinsATT	NP_009230.2:n.788-719_788-717delinsATT
NM_007300.4:c.3780_3782delinsATT	NP_009231.2:p.Leu1260=
NR_027676.2:n.3957_3959delinsATT