Canonical Allele Identifier: CA2260782436

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091930_43091932delinsCCT , CM000679.2:g.43091930_43091932delinsCCT	GRCh38
NC_000017.10:g.41243947_41243949delinsCCT , CM000679.1:g.41243947_41243949delinsCCT	GRCh37
NC_000017.9:g.38497473_38497475delinsCCT	NCBI36
NG_005905.2:g.126052_126054delinsAGG , LRG_292:g.126052_126054delinsAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.3663_3665delinsAGG
ENST00000461574.2:c.3599_3601delinsAGG	ENSP00000417241.2:p.Gln1200=
ENST00000470026.6:c.3599_3601delinsAGG	ENSP00000419274.2:p.Gln1200=
ENST00000473961.6:c.3473_3475delinsAGG	ENSP00000420201.2:p.Gln1158=
ENST00000476777.6:c.3596_3598delinsAGG	ENSP00000417554.2:p.Gln1199=
ENST00000477152.6:c.3521_3523delinsAGG	ENSP00000419988.2:p.Gln1174=
ENST00000478531.6:c.785-900_785-898delinsAGG	ENSP00000420412.2:n.785-900_785-898delinsAGG
ENST00000489037.2:c.3521_3523delinsAGG	ENSP00000420781.2:p.Gln1174=
ENST00000493919.6:c.647-900_647-898delinsAGG	ENSP00000418819.2:n.647-900_647-898delinsAGG
ENST00000494123.6:c.3599_3601delinsAGG	ENSP00000419103.2:p.Gln1200=
ENST00000497488.2:c.2711_2713delinsAGG	ENSP00000418986.2:p.Gln904=
ENST00000618469.2:c.3599_3601delinsAGG	ENSP00000478114.2:p.Gln1200=
ENST00000634433.2:c.3476_3478delinsAGG	ENSP00000489431.2:p.Gln1159=
ENST00000644379.2:c.3599_3601delinsAGG	ENSP00000496570.2:p.Gln1200=
ENST00000644555.2:c.647-900_647-898delinsAGG	ENSP00000494614.2:n.647-900_647-898delinsAGG
ENST00000652672.2:c.3458_3460delinsAGG	ENSP00000498906.2:p.Gln1153=
ENST00000484087.6:c.665-900_665-898delinsAGG	ENSP00000419481.2:n.665-900_665-898delinsAGG
ENST00000700182.1:c.707-900_707-898delinsAGG	ENSP00000514849.1:n.707-900_707-898delinsAGG
ENST00000357654.9:c.3599_3601delinsAGG MANE Select	ENSP00000350283.3:p.Gln1200=
ENST00000471181.7:c.3599_3601delinsAGG	ENSP00000418960.2:p.Gln1200=
ENST00000352993.7:c.671-900_671-898delinsAGG	ENSP00000312236.5:n.671-900_671-898delinsAGG
ENST00000354071.7:c.3599_3601delinsAGG	ENSP00000326002.7:p.Gln1200=
ENST00000357654.7:c.3599_3601delinsAGG	ENSP00000350283.3:p.Gln1200=
ENST00000461221.5:c.*3382_*3384delinsAGG	ENSP00000418548.1:n.*3382_*3384delinsAGG
ENST00000468300.5:c.788-900_788-898delinsAGG	ENSP00000417148.1:n.788-900_788-898delinsAGG
ENST00000471181.6:c.3599_3601delinsAGG	ENSP00000418960.2:p.Gln1200=
ENST00000478531.5:c.785-900_785-898delinsAGG	ENSP00000420412.1:n.785-900_785-898delinsAGG
ENST00000484087.5:c.410-900_410-898delinsAGG	ENSP00000419481.1:n.410-900_410-898delinsAGG
ENST00000487825.5:c.413-900_413-898delinsAGG	ENSP00000418212.1:n.413-900_413-898delinsAGG
ENST00000491747.6:c.788-900_788-898delinsAGG	ENSP00000420705.2:n.788-900_788-898delinsAGG
ENST00000493795.5:c.3458_3460delinsAGG	ENSP00000418775.1:p.Gln1153=
ENST00000493919.5:c.647-900_647-898delinsAGG	ENSP00000418819.1:n.647-900_647-898delinsAGG
ENST00000586385.5:c.5-27981_5-27979delinsAGG	ENSP00000465818.1:n.5-27981_5-27979delinsAGG
ENST00000591534.5:c.-43-17411_-43-17409delinsAGG	ENSP00000467329.1:n.-43-17411_-43-17409delinsAGG
ENST00000591849.5:c.-99+33339_-99+33341delinsAGG	ENSP00000465347.1:n.-99+33339_-99+33341delinsAGG
NM_007294.3:c.3599_3601delinsAGG , LRG_292t1:c.3599_3601delinsAGG	NP_009225.1:p.Gln1200=
NM_007297.3:c.3458_3460delinsAGG	NP_009228.2:p.Gln1153=
NM_007298.3:c.788-900_788-898delinsAGG	NP_009229.2:n.788-900_788-898delinsAGG
NM_007299.3:c.788-900_788-898delinsAGG	NP_009230.2:n.788-900_788-898delinsAGG
NM_007300.3:c.3599_3601delinsAGG	NP_009231.2:p.Gln1200=
NR_027676.1:n.3735_3737delinsAGG
NM_007294.4:c.3599_3601delinsAGG MANE Select	NP_009225.1:p.Gln1200=
NM_007297.4:c.3458_3460delinsAGG	NP_009228.2:p.Gln1153=
NM_007299.4:c.788-900_788-898delinsAGG	NP_009230.2:n.788-900_788-898delinsAGG
NM_007300.4:c.3599_3601delinsAGG	NP_009231.2:p.Gln1200=
NR_027676.2:n.3776_3778delinsAGG