Canonical Allele Identifier: CA2260772815
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43070996T= , CM000679.2:g.43070996T= GRCh38
NC_000017.10:g.41223013T= , CM000679.1:g.41223013T= GRCh37
NC_000017.9:g.38476539T= NCBI36
NG_005905.2:g.146988A= , LRG_292:g.146988A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4915A= ENSP00000417241.2:p.Thr1639=
ENST00000470026.6:c.4918A= ENSP00000419274.2:p.Thr1640=
ENST00000473961.6:c.4792A= ENSP00000420201.2:p.Thr1598=
ENST00000476777.6:c.4912A= ENSP00000417554.2:p.Thr1638=
ENST00000477152.6:c.4840A= ENSP00000419988.2:p.Thr1614=
ENST00000478531.6:c.1606A= ENSP00000420412.2:p.Thr536=
ENST00000489037.2:c.4840A= ENSP00000420781.2:p.Thr1614=
ENST00000493919.6:c.1468A= ENSP00000418819.2:p.Thr490=
ENST00000494123.6:c.4918A= ENSP00000419103.2:p.Thr1640=
ENST00000497488.2:c.4030A= ENSP00000418986.2:p.Thr1344=
ENST00000618469.2:c.4918A= ENSP00000478114.2:p.Thr1640=
ENST00000634433.2:c.4795A= ENSP00000489431.2:p.Thr1599=
ENST00000644379.2:c.4984A= ENSP00000496570.2:p.Thr1662=
ENST00000644555.2:c.1468A= ENSP00000494614.2:p.Thr490=
ENST00000652672.2:c.4777A= ENSP00000498906.2:p.Thr1593=
ENST00000484087.6:c.1480A= ENSP00000419481.2:p.Thr494=
ENST00000700182.1:c.1525A= ENSP00000514849.1:p.Thr509=
ENST00000357654.9:c.4918A= MANE Select ENSP00000350283.3:p.Thr1640=
ENST00000471181.7:c.4981A= ENSP00000418960.2:p.Thr1661=
ENST00000644379.1:c.1305A=
ENST00000352993.7:c.1492A= ENSP00000312236.5:p.Thr498=
ENST00000357654.7:c.4918A= ENSP00000350283.3:p.Thr1640=
ENST00000461221.5:c.*4701A= ENSP00000418548.1:n.*4701A=
ENST00000468300.5:c.1606A= ENSP00000417148.1:p.Thr536=
ENST00000471181.6:c.4981A= ENSP00000418960.2:p.Thr1661=
ENST00000472490.1:n.71A=
ENST00000478531.5:c.1606A= ENSP00000420412.1:p.Thr536=
ENST00000484087.5:c.1231A= ENSP00000419481.1:p.Thr411=
ENST00000491747.6:c.1606A= ENSP00000420705.2:p.Thr536=
ENST00000493795.5:c.4777A= ENSP00000418775.1:p.Thr1593=
ENST00000493919.5:c.1468A= ENSP00000418819.1:p.Thr490=
ENST00000586385.5:c.5-7045A= ENSP00000465818.1:n.5-7045A=
ENST00000591534.5:c.391A= ENSP00000467329.1:p.Thr131=
ENST00000591849.5:c.-98-20806A= ENSP00000465347.1:n.-98-20806A=
NM_007294.3:c.4918A= , LRG_292t1:c.4918A= NP_009225.1:p.Thr1640=
NM_007297.3:c.4777A= NP_009228.2:p.Thr1593=
NM_007298.3:c.1606A= NP_009229.2:p.Thr536=
NM_007299.3:c.1606A= NP_009230.2:p.Thr536=
NM_007300.3:c.4981A= NP_009231.2:p.Thr1661=
NR_027676.1:n.5054A=
NM_007294.4:c.4918A= MANE Select NP_009225.1:p.Thr1640=
NM_007297.4:c.4777A= NP_009228.2:p.Thr1593=
NM_007299.4:c.1606A= NP_009230.2:p.Thr536=
NM_007300.4:c.4981A= NP_009231.2:p.Thr1661=
NR_027676.2:n.5095A=