Canonical Allele Identifier: CA2260775534
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43076586T= , CM000679.2:g.43076586T= GRCh38
NC_000017.10:g.41228603T= , CM000679.1:g.41228603T= GRCh37
NC_000017.9:g.38482129T= NCBI36
NG_005905.2:g.141398A= , LRG_292:g.141398A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4383A= ENSP00000417241.2:p.Glu1461=
ENST00000470026.6:c.4386A= ENSP00000419274.2:p.Glu1462=
ENST00000473961.6:c.4260A= ENSP00000420201.2:p.Glu1420=
ENST00000476777.6:c.4380A= ENSP00000417554.2:p.Glu1460=
ENST00000477152.6:c.4308A= ENSP00000419988.2:p.Glu1436=
ENST00000478531.6:c.1074A= ENSP00000420412.2:p.Glu358=
ENST00000489037.2:c.4308A= ENSP00000420781.2:p.Glu1436=
ENST00000493919.6:c.936A= ENSP00000418819.2:p.Glu312=
ENST00000494123.6:c.4386A= ENSP00000419103.2:p.Glu1462=
ENST00000497488.2:c.3498A= ENSP00000418986.2:p.Glu1166=
ENST00000618469.2:c.4386A= ENSP00000478114.2:p.Glu1462=
ENST00000634433.2:c.4263A= ENSP00000489431.2:p.Glu1421=
ENST00000644379.2:c.4452A= ENSP00000496570.2:p.Glu1484=
ENST00000644555.2:c.936A= ENSP00000494614.2:p.Glu312=
ENST00000652672.2:c.4245A= ENSP00000498906.2:p.Glu1415=
ENST00000484087.6:c.948A= ENSP00000419481.2:p.Glu316=
ENST00000700182.1:c.993A= ENSP00000514849.1:p.Glu331=
ENST00000357654.9:c.4386A= MANE Select ENSP00000350283.3:p.Glu1462=
ENST00000471181.7:c.4449A= ENSP00000418960.2:p.Glu1483=
ENST00000644379.1:c.773A=
ENST00000352993.7:c.960A= ENSP00000312236.5:p.Glu320=
ENST00000357654.7:c.4386A= ENSP00000350283.3:p.Glu1462=
ENST00000461221.5:c.*4169A= ENSP00000418548.1:n.*4169A=
ENST00000461574.1:c.677A=
ENST00000468300.5:c.1074A= ENSP00000417148.1:p.Glu358=
ENST00000471181.6:c.4449A= ENSP00000418960.2:p.Glu1483=
ENST00000478531.5:c.1074A= ENSP00000420412.1:p.Glu358=
ENST00000484087.5:c.699A= ENSP00000419481.1:p.Glu233=
ENST00000487825.5:c.702A= ENSP00000418212.1:p.Glu234=
ENST00000491747.6:c.1074A= ENSP00000420705.2:p.Glu358=
ENST00000493795.5:c.4245A= ENSP00000418775.1:p.Glu1415=
ENST00000493919.5:c.936A= ENSP00000418819.1:p.Glu312=
ENST00000586385.5:c.5-12635A= ENSP00000465818.1:n.5-12635A=
ENST00000591534.5:c.-43-2065A= ENSP00000467329.1:n.-43-2065A=
ENST00000591849.5:c.-98-26396A= ENSP00000465347.1:n.-98-26396A=
ENST00000621897.1:n.277A=
NM_007294.3:c.4386A= , LRG_292t1:c.4386A= NP_009225.1:p.Glu1462=
NM_007297.3:c.4245A= NP_009228.2:p.Glu1415=
NM_007298.3:c.1074A= NP_009229.2:p.Glu358=
NM_007299.3:c.1074A= NP_009230.2:p.Glu358=
NM_007300.3:c.4449A= NP_009231.2:p.Glu1483=
NR_027676.1:n.4522A=
NM_007294.4:c.4386A= MANE Select NP_009225.1:p.Glu1462=
NM_007297.4:c.4245A= NP_009228.2:p.Glu1415=
NM_007299.4:c.1074A= NP_009230.2:p.Glu358=
NM_007300.4:c.4449A= NP_009231.2:p.Glu1483=
NR_027676.2:n.4563A=