Canonical Allele Identifier: CA2260775536
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43076588C= , CM000679.2:g.43076588C= GRCh38
NC_000017.10:g.41228605C= , CM000679.1:g.41228605C= GRCh37
NC_000017.9:g.38482131C= NCBI36
NG_005905.2:g.141396G= , LRG_292:g.141396G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4381G= ENSP00000417241.2:p.Glu1461=
ENST00000470026.6:c.4384G= ENSP00000419274.2:p.Glu1462=
ENST00000473961.6:c.4258G= ENSP00000420201.2:p.Glu1420=
ENST00000476777.6:c.4378G= ENSP00000417554.2:p.Glu1460=
ENST00000477152.6:c.4306G= ENSP00000419988.2:p.Glu1436=
ENST00000478531.6:c.1072G= ENSP00000420412.2:p.Glu358=
ENST00000489037.2:c.4306G= ENSP00000420781.2:p.Glu1436=
ENST00000493919.6:c.934G= ENSP00000418819.2:p.Glu312=
ENST00000494123.6:c.4384G= ENSP00000419103.2:p.Glu1462=
ENST00000497488.2:c.3496G= ENSP00000418986.2:p.Glu1166=
ENST00000618469.2:c.4384G= ENSP00000478114.2:p.Glu1462=
ENST00000634433.2:c.4261G= ENSP00000489431.2:p.Glu1421=
ENST00000644379.2:c.4450G= ENSP00000496570.2:p.Glu1484=
ENST00000644555.2:c.934G= ENSP00000494614.2:p.Glu312=
ENST00000652672.2:c.4243G= ENSP00000498906.2:p.Glu1415=
ENST00000484087.6:c.946G= ENSP00000419481.2:p.Glu316=
ENST00000700182.1:c.991G= ENSP00000514849.1:p.Glu331=
ENST00000357654.9:c.4384G= MANE Select ENSP00000350283.3:p.Glu1462=
ENST00000471181.7:c.4447G= ENSP00000418960.2:p.Glu1483=
ENST00000644379.1:c.771G=
ENST00000352993.7:c.958G= ENSP00000312236.5:p.Glu320=
ENST00000357654.7:c.4384G= ENSP00000350283.3:p.Glu1462=
ENST00000461221.5:c.*4167G= ENSP00000418548.1:n.*4167G=
ENST00000461574.1:c.675G=
ENST00000468300.5:c.1072G= ENSP00000417148.1:p.Glu358=
ENST00000471181.6:c.4447G= ENSP00000418960.2:p.Glu1483=
ENST00000478531.5:c.1072G= ENSP00000420412.1:p.Glu358=
ENST00000484087.5:c.697G= ENSP00000419481.1:p.Glu233=
ENST00000487825.5:c.700G= ENSP00000418212.1:p.Glu234=
ENST00000491747.6:c.1072G= ENSP00000420705.2:p.Glu358=
ENST00000493795.5:c.4243G= ENSP00000418775.1:p.Glu1415=
ENST00000493919.5:c.934G= ENSP00000418819.1:p.Glu312=
ENST00000586385.5:c.5-12637G= ENSP00000465818.1:n.5-12637G=
ENST00000591534.5:c.-43-2067G= ENSP00000467329.1:n.-43-2067G=
ENST00000591849.5:c.-98-26398G= ENSP00000465347.1:n.-98-26398G=
ENST00000621897.1:n.275G=
NM_007294.3:c.4384G= , LRG_292t1:c.4384G= NP_009225.1:p.Glu1462=
NM_007297.3:c.4243G= NP_009228.2:p.Glu1415=
NM_007298.3:c.1072G= NP_009229.2:p.Glu358=
NM_007299.3:c.1072G= NP_009230.2:p.Glu358=
NM_007300.3:c.4447G= NP_009231.2:p.Glu1483=
NR_027676.1:n.4520G=
NM_007294.4:c.4384G= MANE Select NP_009225.1:p.Glu1462=
NM_007297.4:c.4243G= NP_009228.2:p.Glu1415=
NM_007299.4:c.1072G= NP_009230.2:p.Glu358=
NM_007300.4:c.4447G= NP_009231.2:p.Glu1483=
NR_027676.2:n.4561G=