Canonical Allele Identifier: CA2260763714
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43051085C= , CM000679.2:g.43051085C= GRCh38
NC_000017.10:g.41203102C= , CM000679.1:g.41203102C= GRCh37
NC_000017.9:g.38456628C= NCBI36
NG_005905.2:g.166899G= , LRG_292:g.166899G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5307G= ENSP00000417241.2:p.Gly1769=
ENST00000470026.6:c.5310G= ENSP00000419274.2:p.Gly1770=
ENST00000473961.6:c.5184G= ENSP00000420201.2:p.Gly1728=
ENST00000476777.6:c.5304G= ENSP00000417554.2:p.Gly1768=
ENST00000477152.6:c.5232G= ENSP00000419988.2:p.Gly1744=
ENST00000478531.6:c.1998G= ENSP00000420412.2:p.Gly666=
ENST00000489037.2:c.5232G= ENSP00000420781.2:p.Gly1744=
ENST00000493919.6:c.1860G= ENSP00000418819.2:p.Gly620=
ENST00000494123.6:c.5310G= ENSP00000419103.2:p.Gly1770=
ENST00000497488.2:c.4422G= ENSP00000418986.2:p.Gly1474=
ENST00000618469.2:c.5310G= ENSP00000478114.2:p.Gly1770=
ENST00000634433.2:c.5187G= ENSP00000489431.2:p.Gly1729=
ENST00000644379.2:c.5376G= ENSP00000496570.2:p.Gly1792=
ENST00000644555.2:c.1860G= ENSP00000494614.2:p.Gly620=
ENST00000652672.2:c.5169G= ENSP00000498906.2:p.Gly1723=
ENST00000484087.6:c.1872G= ENSP00000419481.2:p.Gly624=
ENST00000357654.9:c.5310G= MANE Select ENSP00000350283.3:p.Gly1770=
ENST00000471181.7:c.5373G= ENSP00000418960.2:p.Gly1791=
ENST00000644379.1:c.1697G=
ENST00000352993.7:c.1884G= ENSP00000312236.5:p.Gly628=
ENST00000357654.7:c.5310G= ENSP00000350283.3:p.Gly1770=
ENST00000461221.5:c.*5093G= ENSP00000418548.1:n.*5093G=
ENST00000468300.5:c.1998G= ENSP00000417148.1:p.Gly666=
ENST00000471181.6:c.5373G= ENSP00000418960.2:p.Gly1791=
ENST00000491747.6:c.1998G= ENSP00000420705.2:p.Gly666=
ENST00000493795.5:c.5169G= ENSP00000418775.1:p.Gly1723=
ENST00000586385.5:c.240G= ENSP00000465818.1:p.Gly80=
ENST00000591534.5:c.783G= ENSP00000467329.1:p.Gly261=
ENST00000591849.5:c.-98-895G= ENSP00000465347.1:n.-98-895G=
NM_007294.3:c.5310G= , LRG_292t1:c.5310G= NP_009225.1:p.Gly1770=
NM_007297.3:c.5169G= NP_009228.2:p.Gly1723=
NM_007298.3:c.1998G= NP_009229.2:p.Gly666=
NM_007299.3:c.1998G= NP_009230.2:p.Gly666=
NM_007300.3:c.5373G= NP_009231.2:p.Gly1791=
NR_027676.1:n.5446G=
NM_007294.4:c.5310G= MANE Select NP_009225.1:p.Gly1770=
NM_007297.4:c.5169G= NP_009228.2:p.Gly1723=
NM_007299.4:c.1998G= NP_009230.2:p.Gly666=
NM_007300.4:c.5373G= NP_009231.2:p.Gly1791=
NR_027676.2:n.5487G=