Canonical Allele Identifier: CA2260760463

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43044826_43044828delinsGCC , CM000679.2:g.43044826_43044828delinsGCC	GRCh38
NC_000017.10:g.41196843_41196845delinsGCC , CM000679.1:g.41196843_41196845delinsGCC	GRCh37
NC_000017.9:g.38450369_38450371delinsGCC	NCBI36
NG_005905.2:g.173156_173158delinsGGC , LRG_292:g.173156_173158delinsGGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.*850_*852delinsGGC	ENSP00000417241.2:n.*850_*852delinsGGC
ENST00000470026.6:c.*850_*852delinsGGC	ENSP00000419274.2:n.*850_*852delinsGGC
ENST00000473961.6:c.*850_*852delinsGGC	ENSP00000420201.2:n.*850_*852delinsGGC
ENST00000476777.6:c.*850_*852delinsGGC	ENSP00000417554.2:n.*850_*852delinsGGC
ENST00000477152.6:c.*850_*852delinsGGC	ENSP00000419988.2:n.*850_*852delinsGGC
ENST00000478531.6:c.*850_*852delinsGGC	ENSP00000420412.2:n.*850_*852delinsGGC
ENST00000489037.2:c.*850_*852delinsGGC	ENSP00000420781.2:n.*850_*852delinsGGC
ENST00000493919.6:c.*850_*852delinsGGC	ENSP00000418819.2:n.*850_*852delinsGGC
ENST00000494123.6:c.*850_*852delinsGGC	ENSP00000419103.2:n.*850_*852delinsGGC
ENST00000497488.2:c.*850_*852delinsGGC	ENSP00000418986.2:n.*850_*852delinsGGC
ENST00000618469.2:c.*850_*852delinsGGC	ENSP00000478114.2:n.*850_*852delinsGGC
ENST00000634433.2:c.*850_*852delinsGGC	ENSP00000489431.2:n.*850_*852delinsGGC
ENST00000644555.2:c.*850_*852delinsGGC	ENSP00000494614.2:n.*850_*852delinsGGC
ENST00000652672.2:c.*850_*852delinsGGC	ENSP00000498906.2:n.*850_*852delinsGGC
ENST00000700081.1:n.2325_2327delinsGGC
ENST00000357654.9:c.*850_*852delinsGGC MANE Select	ENSP00000350283.3:n.*850_*852delinsGGC
ENST00000471181.7:c.*850_*852delinsGGC	ENSP00000418960.2:n.*850_*852delinsGGC
ENST00000352993.7:c.*850_*852delinsGGC	ENSP00000312236.5:n.*850_*852delinsGGC
ENST00000357654.7:c.*850_*852delinsGGC	ENSP00000350283.3:n.*850_*852delinsGGC
ENST00000468300.5:c.*956_*958delinsGGC	ENSP00000417148.1:n.*956_*958delinsGGC
NM_007294.3:c.*850_*852delinsGGC , LRG_292t1:c.*850_*852delinsGGC	NP_009225.1:n.*850_*852delinsGGC
NM_007297.3:c.*850_*852delinsGGC	NP_009228.2:n.*850_*852delinsGGC
NM_007298.3:c.*850_*852delinsGGC	NP_009229.2:n.*850_*852delinsGGC
NM_007299.3:c.*956_*958delinsGGC	NP_009230.2:n.*956_*958delinsGGC
NM_007300.3:c.*850_*852delinsGGC	NP_009231.2:n.*850_*852delinsGGC
NR_027676.1:n.6578_6580delinsGGC
NM_007294.4:c.*850_*852delinsGGC MANE Select	NP_009225.1:n.*850_*852delinsGGC
NM_007297.4:c.*850_*852delinsGGC	NP_009228.2:n.*850_*852delinsGGC
NM_007299.4:c.*956_*958delinsGGC	NP_009230.2:n.*956_*958delinsGGC
NM_007300.4:c.*850_*852delinsGGC	NP_009231.2:n.*850_*852delinsGGC
NR_027676.2:n.6619_6621delinsGGC