Canonical Allele Identifier: CA2260762747
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43049154C= , CM000679.2:g.43049154C= GRCh38
NC_000017.10:g.41201171C= , CM000679.1:g.41201171C= GRCh37
NC_000017.9:g.38454697C= NCBI36
NG_005905.2:g.168830G= , LRG_292:g.168830G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5370G= ENSP00000417241.2:p.Val1790=
ENST00000470026.6:c.5373G= ENSP00000419274.2:p.Val1791=
ENST00000473961.6:c.5247G= ENSP00000420201.2:p.Val1749=
ENST00000476777.6:c.5367G= ENSP00000417554.2:p.Val1789=
ENST00000477152.6:c.5295G= ENSP00000419988.2:p.Val1765=
ENST00000478531.6:c.2061G= ENSP00000420412.2:p.Val687=
ENST00000489037.2:c.5295G= ENSP00000420781.2:p.Val1765=
ENST00000493919.6:c.1923G= ENSP00000418819.2:p.Val641=
ENST00000494123.6:c.5373G= ENSP00000419103.2:p.Val1791=
ENST00000497488.2:c.4485G= ENSP00000418986.2:p.Val1495=
ENST00000618469.2:c.5373G= ENSP00000478114.2:p.Val1791=
ENST00000634433.2:c.5250G= ENSP00000489431.2:p.Val1750=
ENST00000644379.2:c.5439G= ENSP00000496570.2:p.Val1813=
ENST00000644555.2:c.1923G= ENSP00000494614.2:p.Val641=
ENST00000652672.2:c.5232G= ENSP00000498906.2:p.Val1744=
ENST00000484087.6:c.1935G= ENSP00000419481.2:p.Val645=
ENST00000700081.1:n.1256G=
ENST00000357654.9:c.5373G= MANE Select ENSP00000350283.3:p.Val1791=
ENST00000471181.7:c.5436G= ENSP00000418960.2:p.Val1812=
ENST00000644379.1:c.1760G=
ENST00000352993.7:c.1947G= ENSP00000312236.5:p.Val649=
ENST00000357654.7:c.5373G= ENSP00000350283.3:p.Val1791=
ENST00000461221.5:c.*5156G= ENSP00000418548.1:n.*5156G=
ENST00000468300.5:c.2021-1451G= ENSP00000417148.1:n.2021-1451G=
ENST00000471181.6:c.5436G= ENSP00000418960.2:p.Val1812=
ENST00000491747.6:c.2061G= ENSP00000420705.2:p.Val687=
ENST00000493795.5:c.5232G= ENSP00000418775.1:p.Val1744=
ENST00000586385.5:c.303G= ENSP00000465818.1:p.Val101=
ENST00000591534.5:c.846G= ENSP00000467329.1:p.Val282=
ENST00000591849.5:c.72G= ENSP00000465347.1:p.Val24=
NM_007294.3:c.5373G= , LRG_292t1:c.5373G= NP_009225.1:p.Val1791=
NM_007297.3:c.5232G= NP_009228.2:p.Val1744=
NM_007298.3:c.2061G= NP_009229.2:p.Val687=
NM_007299.3:c.2021-1451G= NP_009230.2:n.2021-1451G=
NM_007300.3:c.5436G= NP_009231.2:p.Val1812=
NR_027676.1:n.5509G=
NM_007294.4:c.5373G= MANE Select NP_009225.1:p.Val1791=
NM_007297.4:c.5232G= NP_009228.2:p.Val1744=
NM_007299.4:c.2021-1451G= NP_009230.2:n.2021-1451G=
NM_007300.4:c.5436G= NP_009231.2:p.Val1812=
NR_027676.2:n.5550G=