Canonical Allele Identifier: CA2260771366
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43067651A= , CM000679.2:g.43067651A= GRCh38
NC_000017.10:g.41219668A= , CM000679.1:g.41219668A= GRCh37
NC_000017.9:g.38473194A= NCBI36
NG_005905.2:g.150333T= , LRG_292:g.150333T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5028T= ENSP00000417241.2:p.Thr1676=
ENST00000470026.6:c.5031T= ENSP00000419274.2:p.Thr1677=
ENST00000473961.6:c.4905T= ENSP00000420201.2:p.Thr1635=
ENST00000476777.6:c.5025T= ENSP00000417554.2:p.Thr1675=
ENST00000477152.6:c.4953T= ENSP00000419988.2:p.Thr1651=
ENST00000478531.6:c.1719T= ENSP00000420412.2:p.Thr573=
ENST00000489037.2:c.4953T= ENSP00000420781.2:p.Thr1651=
ENST00000493919.6:c.1581T= ENSP00000418819.2:p.Thr527=
ENST00000494123.6:c.5031T= ENSP00000419103.2:p.Thr1677=
ENST00000497488.2:c.4143T= ENSP00000418986.2:p.Thr1381=
ENST00000618469.2:c.5031T= ENSP00000478114.2:p.Thr1677=
ENST00000634433.2:c.4908T= ENSP00000489431.2:p.Thr1636=
ENST00000644379.2:c.5097T= ENSP00000496570.2:p.Thr1699=
ENST00000644555.2:c.1581T= ENSP00000494614.2:p.Thr527=
ENST00000652672.2:c.4890T= ENSP00000498906.2:p.Thr1630=
ENST00000484087.6:c.1593T= ENSP00000419481.2:p.Thr531=
ENST00000357654.9:c.5031T= MANE Select ENSP00000350283.3:p.Thr1677=
ENST00000471181.7:c.5094T= ENSP00000418960.2:p.Thr1698=
ENST00000644379.1:c.1418T=
ENST00000352993.7:c.1605T= ENSP00000312236.5:p.Thr535=
ENST00000357654.7:c.5031T= ENSP00000350283.3:p.Thr1677=
ENST00000461221.5:c.*4814T= ENSP00000418548.1:n.*4814T=
ENST00000468300.5:c.1719T= ENSP00000417148.1:p.Thr573=
ENST00000471181.6:c.5094T= ENSP00000418960.2:p.Thr1698=
ENST00000472490.1:n.184T=
ENST00000478531.5:c.1719T= ENSP00000420412.1:p.Thr573=
ENST00000484087.5:c.1344T= ENSP00000419481.1:p.Thr448=
ENST00000491747.6:c.1719T= ENSP00000420705.2:p.Thr573=
ENST00000493795.5:c.4890T= ENSP00000418775.1:p.Thr1630=
ENST00000493919.5:c.1581T= ENSP00000418819.1:p.Thr527=
ENST00000586385.5:c.5-3700T= ENSP00000465818.1:n.5-3700T=
ENST00000591534.5:c.504T= ENSP00000467329.1:p.Thr168=
ENST00000591849.5:c.-98-17461T= ENSP00000465347.1:n.-98-17461T=
NM_007294.3:c.5031T= , LRG_292t1:c.5031T= NP_009225.1:p.Thr1677=
NM_007297.3:c.4890T= NP_009228.2:p.Thr1630=
NM_007298.3:c.1719T= NP_009229.2:p.Thr573=
NM_007299.3:c.1719T= NP_009230.2:p.Thr573=
NM_007300.3:c.5094T= NP_009231.2:p.Thr1698=
NR_027676.1:n.5167T=
NM_007294.4:c.5031T= MANE Select NP_009225.1:p.Thr1677=
NM_007297.4:c.4890T= NP_009228.2:p.Thr1630=
NM_007299.4:c.1719T= NP_009230.2:p.Thr573=
NM_007300.4:c.5094T= NP_009231.2:p.Thr1698=
NR_027676.2:n.5208T=