Canonical Allele Identifier: CA2260762019
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43047688C= , CM000679.2:g.43047688C= GRCh38
NC_000017.10:g.41199705C= , CM000679.1:g.41199705C= GRCh37
NC_000017.9:g.38453231C= NCBI36
NG_005905.2:g.170296G= , LRG_292:g.170296G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5419G= ENSP00000417241.2:p.Val1807=
ENST00000470026.6:c.5422G= ENSP00000419274.2:p.Val1808=
ENST00000473961.6:c.5296G= ENSP00000420201.2:p.Val1766=
ENST00000476777.6:c.5416G= ENSP00000417554.2:p.Val1806=
ENST00000477152.6:c.5344G= ENSP00000419988.2:p.Val1782=
ENST00000478531.6:c.2110G= ENSP00000420412.2:p.Val704=
ENST00000489037.2:c.5344G= ENSP00000420781.2:p.Val1782=
ENST00000493919.6:c.1972G= ENSP00000418819.2:p.Val658=
ENST00000494123.6:c.5422G= ENSP00000419103.2:p.Val1808=
ENST00000497488.2:c.4534G= ENSP00000418986.2:p.Val1512=
ENST00000618469.2:c.5422G= ENSP00000478114.2:p.Val1808=
ENST00000634433.2:c.5299G= ENSP00000489431.2:p.Val1767=
ENST00000644379.2:c.5488G= ENSP00000496570.2:p.Val1830=
ENST00000644555.2:c.1972G= ENSP00000494614.2:p.Val658=
ENST00000652672.2:c.5281G= ENSP00000498906.2:p.Val1761=
ENST00000484087.6:c.1984G= ENSP00000419481.2:p.Val662=
ENST00000700081.1:n.1305G=
ENST00000700082.1:n.786G=
ENST00000357654.9:c.5422G= MANE Select ENSP00000350283.3:p.Val1808=
ENST00000471181.7:c.5485G= ENSP00000418960.2:p.Val1829=
ENST00000644379.1:c.1809G=
ENST00000352993.7:c.1996G= ENSP00000312236.5:p.Val666=
ENST00000357654.7:c.5422G= ENSP00000350283.3:p.Val1808=
ENST00000461221.5:c.*5205G= ENSP00000418548.1:n.*5205G=
ENST00000468300.5:c.2036G= ENSP00000417148.1:p.Cys679=
ENST00000471181.6:c.5485G= ENSP00000418960.2:p.Val1829=
ENST00000491747.6:c.2110G= ENSP00000420705.2:p.Val704=
ENST00000493795.5:c.5281G= ENSP00000418775.1:p.Val1761=
ENST00000586385.5:c.352G= ENSP00000465818.1:p.Val118=
ENST00000591534.5:c.895G= ENSP00000467329.1:p.Val299=
ENST00000591849.5:c.121G= ENSP00000465347.1:p.Val41=
NM_007294.3:c.5422G= , LRG_292t1:c.5422G= NP_009225.1:p.Val1808=
NM_007297.3:c.5281G= NP_009228.2:p.Val1761=
NM_007298.3:c.2110G= NP_009229.2:p.Val704=
NM_007299.3:c.2036G= NP_009230.2:p.Cys679=
NM_007300.3:c.5485G= NP_009231.2:p.Val1829=
NR_027676.1:n.5558G=
NM_007294.4:c.5422G= MANE Select NP_009225.1:p.Val1808=
NM_007297.4:c.5281G= NP_009228.2:p.Val1761=
NM_007299.4:c.2036G= NP_009230.2:p.Cys679=
NM_007300.4:c.5485G= NP_009231.2:p.Val1829=
NR_027676.2:n.5599G=