Canonical Allele Identifier: CA2260778080

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082562A= , CM000679.2:g.43082562A=	GRCh38
NC_000017.10:g.41234579A= , CM000679.1:g.41234579A=	GRCh37
NC_000017.9:g.38488105A=	NCBI36
NG_005905.2:g.135422T= , LRG_292:g.135422T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4199T=	ENSP00000417241.2:p.Met1400=
ENST00000470026.6:c.4199T=	ENSP00000419274.2:p.Met1400=
ENST00000473961.6:c.4073T=	ENSP00000420201.2:p.Met1358=
ENST00000476777.6:c.4193T=	ENSP00000417554.2:p.Met1398=
ENST00000477152.6:c.4121T=	ENSP00000419988.2:p.Met1374=
ENST00000478531.6:c.887T=	ENSP00000420412.2:p.Met296=
ENST00000489037.2:c.4121T=	ENSP00000420781.2:p.Met1374=
ENST00000493919.6:c.749T=	ENSP00000418819.2:p.Met250=
ENST00000494123.6:c.4199T=	ENSP00000419103.2:p.Met1400=
ENST00000497488.2:c.3311T=	ENSP00000418986.2:p.Met1104=
ENST00000618469.2:c.4199T=	ENSP00000478114.2:p.Met1400=
ENST00000634433.2:c.4076T=	ENSP00000489431.2:p.Met1359=
ENST00000644379.2:c.4199T=	ENSP00000496570.2:p.Met1400=
ENST00000644555.2:c.749T=	ENSP00000494614.2:p.Met250=
ENST00000652672.2:c.4058T=	ENSP00000498906.2:p.Met1353=
ENST00000484087.6:c.764T=	ENSP00000419481.2:p.Met255=
ENST00000700182.1:c.809T=	ENSP00000514849.1:p.Met270=
ENST00000357654.9:c.4199T= MANE Select	ENSP00000350283.3:p.Met1400=
ENST00000471181.7:c.4199T=	ENSP00000418960.2:p.Met1400=
ENST00000644379.1:c.520T=
ENST00000352993.7:c.773T=	ENSP00000312236.5:p.Met258=
ENST00000357654.7:c.4199T=	ENSP00000350283.3:p.Met1400=
ENST00000461221.5:c.*3982T=	ENSP00000418548.1:n.*3982T=
ENST00000461574.1:c.493T=
ENST00000468300.5:c.890T=	ENSP00000417148.1:p.Met297=
ENST00000471181.6:c.4199T=	ENSP00000418960.2:p.Met1400=
ENST00000478531.5:c.887T=	ENSP00000420412.1:p.Met296=
ENST00000484087.5:c.512T=	ENSP00000419481.1:p.Met171=
ENST00000487825.5:c.515T=	ENSP00000418212.1:p.Met172=
ENST00000491747.6:c.890T=	ENSP00000420705.2:p.Met297=
ENST00000493795.5:c.4058T=	ENSP00000418775.1:p.Met1353=
ENST00000493919.5:c.749T=	ENSP00000418819.1:p.Met250=
ENST00000586385.5:c.5-18611T=	ENSP00000465818.1:n.5-18611T=
ENST00000591534.5:c.-43-8041T=	ENSP00000467329.1:n.-43-8041T=
ENST00000591849.5:c.-98-32372T=	ENSP00000465347.1:n.-98-32372T=
ENST00000621897.1:n.93T=
NM_007294.3:c.4199T= , LRG_292t1:c.4199T=	NP_009225.1:p.Met1400=
NM_007297.3:c.4058T=	NP_009228.2:p.Met1353=
NM_007298.3:c.890T=	NP_009229.2:p.Met297=
NM_007299.3:c.890T=	NP_009230.2:p.Met297=
NM_007300.3:c.4199T=	NP_009231.2:p.Met1400=
NR_027676.1:n.4335T=
NM_007294.4:c.4199T= MANE Select	NP_009225.1:p.Met1400=
NM_007297.4:c.4058T=	NP_009228.2:p.Met1353=
NM_007299.4:c.890T=	NP_009230.2:p.Met297=
NM_007300.4:c.4199T=	NP_009231.2:p.Met1400=
NR_027676.2:n.4376T=