Canonical Allele Identifier: CA2260783045

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092548_43092550delinsTAC , CM000679.2:g.43092548_43092550delinsTAC	GRCh38
NC_000017.10:g.41244565_41244567delinsTAC , CM000679.1:g.41244565_41244567delinsTAC	GRCh37
NC_000017.9:g.38498091_38498093delinsTAC	NCBI36
NG_005905.2:g.125434_125436delinsGTA , LRG_292:g.125434_125436delinsGTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.3045_3047delinsGTA
ENST00000461574.2:c.2981_2983delinsGTA	ENSP00000417241.2:p.Cys994=
ENST00000470026.6:c.2981_2983delinsGTA	ENSP00000419274.2:p.Cys994=
ENST00000473961.6:c.2855_2857delinsGTA	ENSP00000420201.2:p.Cys952=
ENST00000476777.6:c.2978_2980delinsGTA	ENSP00000417554.2:p.Cys993=
ENST00000477152.6:c.2903_2905delinsGTA	ENSP00000419988.2:p.Cys968=
ENST00000478531.6:c.785-1518_785-1516delinsGTA	ENSP00000420412.2:n.785-1518_785-1516delinsGTA
ENST00000489037.2:c.2903_2905delinsGTA	ENSP00000420781.2:p.Cys968=
ENST00000493919.6:c.647-1518_647-1516delinsGTA	ENSP00000418819.2:n.647-1518_647-1516delinsGTA
ENST00000494123.6:c.2981_2983delinsGTA	ENSP00000419103.2:p.Cys994=
ENST00000497488.2:c.2093_2095delinsGTA	ENSP00000418986.2:p.Cys698=
ENST00000618469.2:c.2981_2983delinsGTA	ENSP00000478114.2:p.Cys994=
ENST00000634433.2:c.2858_2860delinsGTA	ENSP00000489431.2:p.Cys953=
ENST00000644379.2:c.2981_2983delinsGTA	ENSP00000496570.2:p.Cys994=
ENST00000644555.2:c.647-1518_647-1516delinsGTA	ENSP00000494614.2:n.647-1518_647-1516delinsGTA
ENST00000652672.2:c.2840_2842delinsGTA	ENSP00000498906.2:p.Cys947=
ENST00000484087.6:c.665-1518_665-1516delinsGTA	ENSP00000419481.2:n.665-1518_665-1516delinsGTA
ENST00000700182.1:c.707-1518_707-1516delinsGTA	ENSP00000514849.1:n.707-1518_707-1516delinsGTA
ENST00000357654.9:c.2981_2983delinsGTA MANE Select	ENSP00000350283.3:p.Cys994=
ENST00000471181.7:c.2981_2983delinsGTA	ENSP00000418960.2:p.Cys994=
ENST00000352993.7:c.671-1518_671-1516delinsGTA	ENSP00000312236.5:n.671-1518_671-1516delinsGTA
ENST00000354071.7:c.2981_2983delinsGTA	ENSP00000326002.7:p.Cys994=
ENST00000357654.7:c.2981_2983delinsGTA	ENSP00000350283.3:p.Cys994=
ENST00000461221.5:c.*2764_*2766delinsGTA	ENSP00000418548.1:n.*2764_*2766delinsGTA
ENST00000468300.5:c.788-1518_788-1516delinsGTA	ENSP00000417148.1:n.788-1518_788-1516delinsGTA
ENST00000471181.6:c.2981_2983delinsGTA	ENSP00000418960.2:p.Cys994=
ENST00000478531.5:c.785-1518_785-1516delinsGTA	ENSP00000420412.1:n.785-1518_785-1516delinsGTA
ENST00000484087.5:c.410-1518_410-1516delinsGTA	ENSP00000419481.1:n.410-1518_410-1516delinsGTA
ENST00000487825.5:c.413-1518_413-1516delinsGTA	ENSP00000418212.1:n.413-1518_413-1516delinsGTA
ENST00000491747.6:c.788-1518_788-1516delinsGTA	ENSP00000420705.2:n.788-1518_788-1516delinsGTA
ENST00000493795.5:c.2840_2842delinsGTA	ENSP00000418775.1:p.Cys947=
ENST00000493919.5:c.647-1518_647-1516delinsGTA	ENSP00000418819.1:n.647-1518_647-1516delinsGTA
ENST00000586385.5:c.5-28599_5-28597delinsGTA	ENSP00000465818.1:n.5-28599_5-28597delinsGTA
ENST00000591534.5:c.-43-18029_-43-18027delinsGTA	ENSP00000467329.1:n.-43-18029_-43-18027delinsGTA
ENST00000591849.5:c.-99+32721_-99+32723delinsGTA	ENSP00000465347.1:n.-99+32721_-99+32723delinsGTA
NM_007294.3:c.2981_2983delinsGTA , LRG_292t1:c.2981_2983delinsGTA	NP_009225.1:p.Cys994=
NM_007297.3:c.2840_2842delinsGTA	NP_009228.2:p.Cys947=
NM_007298.3:c.788-1518_788-1516delinsGTA	NP_009229.2:n.788-1518_788-1516delinsGTA
NM_007299.3:c.788-1518_788-1516delinsGTA	NP_009230.2:n.788-1518_788-1516delinsGTA
NM_007300.3:c.2981_2983delinsGTA	NP_009231.2:p.Cys994=
NR_027676.1:n.3117_3119delinsGTA
NM_007294.4:c.2981_2983delinsGTA MANE Select	NP_009225.1:p.Cys994=
NM_007297.4:c.2840_2842delinsGTA	NP_009228.2:p.Cys947=
NM_007299.4:c.788-1518_788-1516delinsGTA	NP_009230.2:n.788-1518_788-1516delinsGTA
NM_007300.4:c.2981_2983delinsGTA	NP_009231.2:p.Cys994=
NR_027676.2:n.3158_3160delinsGTA