Canonical Allele Identifier: CA2260781609

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43090923A= , CM000679.2:g.43090923A=	GRCh38
NC_000017.10:g.41242940A= , CM000679.1:g.41242940A=	GRCh37
NC_000017.9:g.38496466A=	NCBI36
NG_005905.2:g.127061T= , LRG_292:g.127061T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4185+21T=	ENSP00000417241.2:n.4185+21T=
ENST00000470026.6:c.4185+21T=	ENSP00000419274.2:n.4185+21T=
ENST00000473961.6:c.4059+21T=	ENSP00000420201.2:n.4059+21T=
ENST00000476777.6:c.4182+21T=	ENSP00000417554.2:n.4182+21T=
ENST00000477152.6:c.4107+21T=	ENSP00000419988.2:n.4107+21T=
ENST00000478531.6:c.873+21T=	ENSP00000420412.2:n.873+21T=
ENST00000489037.2:c.4107+21T=	ENSP00000420781.2:n.4107+21T=
ENST00000493919.6:c.735+21T=	ENSP00000418819.2:n.735+21T=
ENST00000494123.6:c.4185+21T=	ENSP00000419103.2:n.4185+21T=
ENST00000497488.2:c.3297+21T=	ENSP00000418986.2:n.3297+21T=
ENST00000618469.2:c.4185+21T=	ENSP00000478114.2:n.4185+21T=
ENST00000634433.2:c.4062+21T=	ENSP00000489431.2:n.4062+21T=
ENST00000644379.2:c.4185+21T=	ENSP00000496570.2:n.4185+21T=
ENST00000644555.2:c.735+21T=	ENSP00000494614.2:n.735+21T=
ENST00000652672.2:c.4044+21T=	ENSP00000498906.2:n.4044+21T=
ENST00000484087.6:c.753+21T=	ENSP00000419481.2:n.753+21T=
ENST00000700182.1:c.795+21T=	ENSP00000514849.1:n.795+21T=
ENST00000357654.9:c.4185+21T= MANE Select	ENSP00000350283.3:n.4185+21T=
ENST00000471181.7:c.4185+21T=	ENSP00000418960.2:n.4185+21T=
ENST00000644379.1:c.506+21T=
ENST00000352993.7:c.759+21T=	ENSP00000312236.5:n.759+21T=
ENST00000357654.7:c.4185+21T=	ENSP00000350283.3:n.4185+21T=
ENST00000461221.5:c.*3968+21T=	ENSP00000418548.1:n.*3968+21T=
ENST00000461574.1:c.479+21T=
ENST00000468300.5:c.876+21T=	ENSP00000417148.1:n.876+21T=
ENST00000471181.6:c.4185+21T=	ENSP00000418960.2:n.4185+21T=
ENST00000478531.5:c.873+21T=	ENSP00000420412.1:n.873+21T=
ENST00000484087.5:c.498+21T=	ENSP00000419481.1:n.498+21T=
ENST00000487825.5:c.501+21T=	ENSP00000418212.1:n.501+21T=
ENST00000491747.6:c.876+21T=	ENSP00000420705.2:n.876+21T=
ENST00000493795.5:c.4044+21T=	ENSP00000418775.1:n.4044+21T=
ENST00000493919.5:c.735+21T=	ENSP00000418819.1:n.735+21T=
ENST00000586385.5:c.5-26972T=	ENSP00000465818.1:n.5-26972T=
ENST00000591534.5:c.-43-16402T=	ENSP00000467329.1:n.-43-16402T=
ENST00000591849.5:c.-99+34348T=	ENSP00000465347.1:n.-99+34348T=
NM_007294.3:c.4185+21T= , LRG_292t1:c.4185+21T=	NP_009225.1:n.4185+21T=
NM_007297.3:c.4044+21T=	NP_009228.2:n.4044+21T=
NM_007298.3:c.876+21T=	NP_009229.2:n.876+21T=
NM_007299.3:c.876+21T=	NP_009230.2:n.876+21T=
NM_007300.3:c.4185+21T=	NP_009231.2:n.4185+21T=
NR_027676.1:n.4321+21T=
NM_007294.4:c.4185+21T= MANE Select	NP_009225.1:n.4185+21T=
NM_007297.4:c.4044+21T=	NP_009228.2:n.4044+21T=
NM_007299.4:c.876+21T=	NP_009230.2:n.876+21T=
NM_007300.4:c.4185+21T=	NP_009231.2:n.4185+21T=
NR_027676.2:n.4362+21T=