Canonical Allele Identifier: CA2260763710
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43051077G= , CM000679.2:g.43051077G= GRCh38
NC_000017.10:g.41203094G= , CM000679.1:g.41203094G= GRCh37
NC_000017.9:g.38456620G= NCBI36
NG_005905.2:g.166907C= , LRG_292:g.166907C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5315C= ENSP00000417241.2:p.Thr1772=
ENST00000470026.6:c.5318C= ENSP00000419274.2:p.Thr1773=
ENST00000473961.6:c.5192C= ENSP00000420201.2:p.Thr1731=
ENST00000476777.6:c.5312C= ENSP00000417554.2:p.Thr1771=
ENST00000477152.6:c.5240C= ENSP00000419988.2:p.Thr1747=
ENST00000478531.6:c.2006C= ENSP00000420412.2:p.Thr669=
ENST00000489037.2:c.5240C= ENSP00000420781.2:p.Thr1747=
ENST00000493919.6:c.1868C= ENSP00000418819.2:p.Thr623=
ENST00000494123.6:c.5318C= ENSP00000419103.2:p.Thr1773=
ENST00000497488.2:c.4430C= ENSP00000418986.2:p.Thr1477=
ENST00000618469.2:c.5318C= ENSP00000478114.2:p.Thr1773=
ENST00000634433.2:c.5195C= ENSP00000489431.2:p.Thr1732=
ENST00000644379.2:c.5384C= ENSP00000496570.2:p.Thr1795=
ENST00000644555.2:c.1868C= ENSP00000494614.2:p.Thr623=
ENST00000652672.2:c.5177C= ENSP00000498906.2:p.Thr1726=
ENST00000484087.6:c.1880C= ENSP00000419481.2:p.Thr627=
ENST00000357654.9:c.5318C= MANE Select ENSP00000350283.3:p.Thr1773=
ENST00000471181.7:c.5381C= ENSP00000418960.2:p.Thr1794=
ENST00000644379.1:c.1705C=
ENST00000352993.7:c.1892C= ENSP00000312236.5:p.Thr631=
ENST00000357654.7:c.5318C= ENSP00000350283.3:p.Thr1773=
ENST00000461221.5:c.*5101C= ENSP00000418548.1:n.*5101C=
ENST00000468300.5:c.2006C= ENSP00000417148.1:p.Thr669=
ENST00000471181.6:c.5381C= ENSP00000418960.2:p.Thr1794=
ENST00000491747.6:c.2006C= ENSP00000420705.2:p.Thr669=
ENST00000493795.5:c.5177C= ENSP00000418775.1:p.Thr1726=
ENST00000586385.5:c.248C= ENSP00000465818.1:p.Thr83=
ENST00000591534.5:c.791C= ENSP00000467329.1:p.Thr264=
ENST00000591849.5:c.-98-887C= ENSP00000465347.1:n.-98-887C=
NM_007294.3:c.5318C= , LRG_292t1:c.5318C= NP_009225.1:p.Thr1773=
NM_007297.3:c.5177C= NP_009228.2:p.Thr1726=
NM_007298.3:c.2006C= NP_009229.2:p.Thr669=
NM_007299.3:c.2006C= NP_009230.2:p.Thr669=
NM_007300.3:c.5381C= NP_009231.2:p.Thr1794=
NR_027676.1:n.5454C=
NM_007294.4:c.5318C= MANE Select NP_009225.1:p.Thr1773=
NM_007297.4:c.5177C= NP_009228.2:p.Thr1726=
NM_007299.4:c.2006C= NP_009230.2:p.Thr669=
NM_007300.4:c.5381C= NP_009231.2:p.Thr1794=
NR_027676.2:n.5495C=