Canonical Allele Identifier: CA2260761067
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045731A= , CM000679.2:g.43045731A= GRCh38
NC_000017.10:g.41197748A= , CM000679.1:g.41197748A= GRCh37
NC_000017.9:g.38451274A= NCBI36
NG_005905.2:g.172253T= , LRG_292:g.172253T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5536T= ENSP00000417241.2:p.Cys1846=
ENST00000470026.6:c.5539T= ENSP00000419274.2:p.Cys1847=
ENST00000473961.6:c.5413T= ENSP00000420201.2:p.Cys1805=
ENST00000476777.6:c.5533T= ENSP00000417554.2:p.Cys1845=
ENST00000477152.6:c.5461T= ENSP00000419988.2:p.Cys1821=
ENST00000478531.6:c.2227T= ENSP00000420412.2:p.Cys743=
ENST00000489037.2:c.5461T= ENSP00000420781.2:p.Cys1821=
ENST00000493919.6:c.2089T= ENSP00000418819.2:p.Cys697=
ENST00000494123.6:c.5539T= ENSP00000419103.2:p.Cys1847=
ENST00000497488.2:c.4651T= ENSP00000418986.2:p.Cys1551=
ENST00000618469.2:c.5539T= ENSP00000478114.2:p.Cys1847=
ENST00000634433.2:c.5416T= ENSP00000489431.2:p.Cys1806=
ENST00000644379.2:c.5605T= ENSP00000496570.2:p.Cys1869=
ENST00000644555.2:c.2089T= ENSP00000494614.2:p.Cys697=
ENST00000652672.2:c.5398T= ENSP00000498906.2:p.Cys1800=
ENST00000484087.6:c.2101T= ENSP00000419481.2:p.Cys701=
ENST00000700081.1:n.1422T=
ENST00000700082.1:n.903T=
ENST00000357654.9:c.5539T= MANE Select ENSP00000350283.3:p.Cys1847=
ENST00000471181.7:c.5602T= ENSP00000418960.2:p.Cys1868=
ENST00000644379.1:c.1926T=
ENST00000352993.7:c.2113T= ENSP00000312236.5:p.Cys705=
ENST00000357654.7:c.5539T= ENSP00000350283.3:p.Cys1847=
ENST00000461221.5:c.*5322T= ENSP00000418548.1:n.*5322T=
ENST00000468300.5:c.*53T= ENSP00000417148.1:n.*53T=
ENST00000471181.6:c.5602T= ENSP00000418960.2:p.Cys1868=
ENST00000491747.6:c.2227T= ENSP00000420705.2:p.Cys743=
ENST00000493795.5:c.5398T= ENSP00000418775.1:p.Cys1800=
ENST00000586385.5:c.469T= ENSP00000465818.1:p.Cys157=
ENST00000591534.5:c.1012T= ENSP00000467329.1:p.Cys338=
ENST00000591849.5:c.238T= ENSP00000465347.1:p.Cys80=
NM_007294.3:c.5539T= , LRG_292t1:c.5539T= NP_009225.1:p.Cys1847=
NM_007297.3:c.5398T= NP_009228.2:p.Cys1800=
NM_007298.3:c.2227T= NP_009229.2:p.Cys743=
NM_007299.3:c.*53T= NP_009230.2:n.*53T=
NM_007300.3:c.5602T= NP_009231.2:p.Cys1868=
NR_027676.1:n.5675T=
NM_007294.4:c.5539T= MANE Select NP_009225.1:p.Cys1847=
NM_007297.4:c.5398T= NP_009228.2:p.Cys1800=
NM_007299.4:c.*53T= NP_009230.2:n.*53T=
NM_007300.4:c.5602T= NP_009231.2:p.Cys1868=
NR_027676.2:n.5716T=