Canonical Allele Identifier: CA2260762889

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43049376A= , CM000679.2:g.43049376A=	GRCh38
NC_000017.10:g.41201393A= , CM000679.1:g.41201393A=	GRCh37
NC_000017.9:g.38454919A=	NCBI36
NG_005905.2:g.168608T= , LRG_292:g.168608T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5330-182T=	ENSP00000417241.2:n.5330-182T=
ENST00000470026.6:c.5333-182T=	ENSP00000419274.2:n.5333-182T=
ENST00000473961.6:c.5207-182T=	ENSP00000420201.2:n.5207-182T=
ENST00000476777.6:c.5327-182T=	ENSP00000417554.2:n.5327-182T=
ENST00000477152.6:c.5255-182T=	ENSP00000419988.2:n.5255-182T=
ENST00000478531.6:c.2021-182T=	ENSP00000420412.2:n.2021-182T=
ENST00000489037.2:c.5255-182T=	ENSP00000420781.2:n.5255-182T=
ENST00000493919.6:c.1883-182T=	ENSP00000418819.2:n.1883-182T=
ENST00000494123.6:c.5333-182T=	ENSP00000419103.2:n.5333-182T=
ENST00000497488.2:c.4445-182T=	ENSP00000418986.2:n.4445-182T=
ENST00000618469.2:c.5333-182T=	ENSP00000478114.2:n.5333-182T=
ENST00000634433.2:c.5210-182T=	ENSP00000489431.2:n.5210-182T=
ENST00000644379.2:c.5399-182T=	ENSP00000496570.2:n.5399-182T=
ENST00000644555.2:c.1883-182T=	ENSP00000494614.2:n.1883-182T=
ENST00000652672.2:c.5192-182T=	ENSP00000498906.2:n.5192-182T=
ENST00000484087.6:c.1895-182T=	ENSP00000419481.2:n.1895-182T=
ENST00000700081.1:n.1034T=
ENST00000357654.9:c.5333-182T= MANE Select	ENSP00000350283.3:n.5333-182T=
ENST00000471181.7:c.5396-182T=	ENSP00000418960.2:n.5396-182T=
ENST00000644379.1:c.1720-182T=
ENST00000352993.7:c.1907-182T=	ENSP00000312236.5:n.1907-182T=
ENST00000357654.7:c.5333-182T=	ENSP00000350283.3:n.5333-182T=
ENST00000461221.5:c.*5116-182T=	ENSP00000418548.1:n.*5116-182T=
ENST00000468300.5:c.2021-1673T=	ENSP00000417148.1:n.2021-1673T=
ENST00000471181.6:c.5396-182T=	ENSP00000418960.2:n.5396-182T=
ENST00000491747.6:c.2021-182T=	ENSP00000420705.2:n.2021-182T=
ENST00000493795.5:c.5192-182T=	ENSP00000418775.1:n.5192-182T=
ENST00000586385.5:c.263-182T=	ENSP00000465818.1:n.263-182T=
ENST00000591534.5:c.806-182T=	ENSP00000467329.1:n.806-182T=
ENST00000591849.5:c.32-182T=	ENSP00000465347.1:n.32-182T=
NM_007294.3:c.5333-182T= , LRG_292t1:c.5333-182T=	NP_009225.1:n.5333-182T=
NM_007297.3:c.5192-182T=	NP_009228.2:n.5192-182T=
NM_007298.3:c.2021-182T=	NP_009229.2:n.2021-182T=
NM_007299.3:c.2021-1673T=	NP_009230.2:n.2021-1673T=
NM_007300.3:c.5396-182T=	NP_009231.2:n.5396-182T=
NR_027676.1:n.5469-182T=
NM_007294.4:c.5333-182T= MANE Select	NP_009225.1:n.5333-182T=
NM_007297.4:c.5192-182T=	NP_009228.2:n.5192-182T=
NM_007299.4:c.2021-1673T=	NP_009230.2:n.2021-1673T=
NM_007300.4:c.5396-182T=	NP_009231.2:n.5396-182T=
NR_027676.2:n.5510-182T=