Canonical Allele Identifier: CA2260782724

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092213_43092214delinsAG , CM000679.2:g.43092213_43092214delinsAG	GRCh38
NC_000017.10:g.41244230_41244231delinsAG , CM000679.1:g.41244230_41244231delinsAG	GRCh37
NC_000017.9:g.38497756_38497757delinsAG	NCBI36
NG_005905.2:g.125770_125771delinsCT , LRG_292:g.125770_125771delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3381_3382delinsCT
ENST00000461574.2:c.3317_3318delinsCT	ENSP00000417241.2:p.Pro1106=
ENST00000470026.6:c.3317_3318delinsCT	ENSP00000419274.2:p.Pro1106=
ENST00000473961.6:c.3191_3192delinsCT	ENSP00000420201.2:p.Pro1064=
ENST00000476777.6:c.3314_3315delinsCT	ENSP00000417554.2:p.Pro1105=
ENST00000477152.6:c.3239_3240delinsCT	ENSP00000419988.2:p.Pro1080=
ENST00000478531.6:c.785-1182_785-1181delinsCT	ENSP00000420412.2:n.785-1182_785-1181delinsCT
ENST00000489037.2:c.3239_3240delinsCT	ENSP00000420781.2:p.Pro1080=
ENST00000493919.6:c.647-1182_647-1181delinsCT	ENSP00000418819.2:n.647-1182_647-1181delinsCT
ENST00000494123.6:c.3317_3318delinsCT	ENSP00000419103.2:p.Pro1106=
ENST00000497488.2:c.2429_2430delinsCT	ENSP00000418986.2:p.Pro810=
ENST00000618469.2:c.3317_3318delinsCT	ENSP00000478114.2:p.Pro1106=
ENST00000634433.2:c.3194_3195delinsCT	ENSP00000489431.2:p.Pro1065=
ENST00000644379.2:c.3317_3318delinsCT	ENSP00000496570.2:p.Pro1106=
ENST00000644555.2:c.647-1182_647-1181delinsCT	ENSP00000494614.2:n.647-1182_647-1181delinsCT
ENST00000652672.2:c.3176_3177delinsCT	ENSP00000498906.2:p.Pro1059=
ENST00000484087.6:c.665-1182_665-1181delinsCT	ENSP00000419481.2:n.665-1182_665-1181delinsCT
ENST00000700182.1:c.707-1182_707-1181delinsCT	ENSP00000514849.1:n.707-1182_707-1181delinsCT
ENST00000357654.9:c.3317_3318delinsCT MANE Select	ENSP00000350283.3:p.Pro1106=
ENST00000471181.7:c.3317_3318delinsCT	ENSP00000418960.2:p.Pro1106=
ENST00000352993.7:c.671-1182_671-1181delinsCT	ENSP00000312236.5:n.671-1182_671-1181delinsCT
ENST00000354071.7:c.3317_3318delinsCT	ENSP00000326002.7:p.Pro1106=
ENST00000357654.7:c.3317_3318delinsCT	ENSP00000350283.3:p.Pro1106=
ENST00000461221.5:c.*3100_*3101delinsCT	ENSP00000418548.1:n.*3100_*3101delinsCT
ENST00000468300.5:c.788-1182_788-1181delinsCT	ENSP00000417148.1:n.788-1182_788-1181delinsCT
ENST00000471181.6:c.3317_3318delinsCT	ENSP00000418960.2:p.Pro1106=
ENST00000478531.5:c.785-1182_785-1181delinsCT	ENSP00000420412.1:n.785-1182_785-1181delinsCT
ENST00000484087.5:c.410-1182_410-1181delinsCT	ENSP00000419481.1:n.410-1182_410-1181delinsCT
ENST00000487825.5:c.413-1182_413-1181delinsCT	ENSP00000418212.1:n.413-1182_413-1181delinsCT
ENST00000491747.6:c.788-1182_788-1181delinsCT	ENSP00000420705.2:n.788-1182_788-1181delinsCT
ENST00000493795.5:c.3176_3177delinsCT	ENSP00000418775.1:p.Pro1059=
ENST00000493919.5:c.647-1182_647-1181delinsCT	ENSP00000418819.1:n.647-1182_647-1181delinsCT
ENST00000586385.5:c.5-28263_5-28262delinsCT	ENSP00000465818.1:n.5-28263_5-28262delinsCT
ENST00000591534.5:c.-43-17693_-43-17692delinsCT	ENSP00000467329.1:n.-43-17693_-43-17692delinsCT
ENST00000591849.5:c.-99+33057_-99+33058delinsCT	ENSP00000465347.1:n.-99+33057_-99+33058delinsCT
NM_007294.3:c.3317_3318delinsCT , LRG_292t1:c.3317_3318delinsCT	NP_009225.1:p.Pro1106=
NM_007297.3:c.3176_3177delinsCT	NP_009228.2:p.Pro1059=
NM_007298.3:c.788-1182_788-1181delinsCT	NP_009229.2:n.788-1182_788-1181delinsCT
NM_007299.3:c.788-1182_788-1181delinsCT	NP_009230.2:n.788-1182_788-1181delinsCT
NM_007300.3:c.3317_3318delinsCT	NP_009231.2:p.Pro1106=
NR_027676.1:n.3453_3454delinsCT
NM_007294.4:c.3317_3318delinsCT MANE Select	NP_009225.1:p.Pro1106=
NM_007297.4:c.3176_3177delinsCT	NP_009228.2:p.Pro1059=
NM_007299.4:c.788-1182_788-1181delinsCT	NP_009230.2:n.788-1182_788-1181delinsCT
NM_007300.4:c.3317_3318delinsCT	NP_009231.2:p.Pro1106=
NR_027676.2:n.3494_3495delinsCT