Canonical Allele Identifier: CA2260775527
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43076581G= , CM000679.2:g.43076581G= GRCh38
NC_000017.10:g.41228598G= , CM000679.1:g.41228598G= GRCh37
NC_000017.9:g.38482124G= NCBI36
NG_005905.2:g.141403C= , LRG_292:g.141403C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4388C= ENSP00000417241.2:p.Pro1463=
ENST00000470026.6:c.4391C= ENSP00000419274.2:p.Pro1464=
ENST00000473961.6:c.4265C= ENSP00000420201.2:p.Pro1422=
ENST00000476777.6:c.4385C= ENSP00000417554.2:p.Pro1462=
ENST00000477152.6:c.4313C= ENSP00000419988.2:p.Pro1438=
ENST00000478531.6:c.1079C= ENSP00000420412.2:p.Pro360=
ENST00000489037.2:c.4313C= ENSP00000420781.2:p.Pro1438=
ENST00000493919.6:c.941C= ENSP00000418819.2:p.Pro314=
ENST00000494123.6:c.4391C= ENSP00000419103.2:p.Pro1464=
ENST00000497488.2:c.3503C= ENSP00000418986.2:p.Pro1168=
ENST00000618469.2:c.4391C= ENSP00000478114.2:p.Pro1464=
ENST00000634433.2:c.4268C= ENSP00000489431.2:p.Pro1423=
ENST00000644379.2:c.4457C= ENSP00000496570.2:p.Pro1486=
ENST00000644555.2:c.941C= ENSP00000494614.2:p.Pro314=
ENST00000652672.2:c.4250C= ENSP00000498906.2:p.Pro1417=
ENST00000484087.6:c.953C= ENSP00000419481.2:p.Pro318=
ENST00000700182.1:c.998C= ENSP00000514849.1:p.Pro333=
ENST00000357654.9:c.4391C= MANE Select ENSP00000350283.3:p.Pro1464=
ENST00000471181.7:c.4454C= ENSP00000418960.2:p.Pro1485=
ENST00000644379.1:c.778C=
ENST00000352993.7:c.965C= ENSP00000312236.5:p.Pro322=
ENST00000357654.7:c.4391C= ENSP00000350283.3:p.Pro1464=
ENST00000461221.5:c.*4174C= ENSP00000418548.1:n.*4174C=
ENST00000461574.1:c.682C=
ENST00000468300.5:c.1079C= ENSP00000417148.1:p.Pro360=
ENST00000471181.6:c.4454C= ENSP00000418960.2:p.Pro1485=
ENST00000478531.5:c.1079C= ENSP00000420412.1:p.Pro360=
ENST00000484087.5:c.704C= ENSP00000419481.1:p.Pro235=
ENST00000487825.5:c.707C= ENSP00000418212.1:p.Pro236=
ENST00000491747.6:c.1079C= ENSP00000420705.2:p.Pro360=
ENST00000493795.5:c.4250C= ENSP00000418775.1:p.Pro1417=
ENST00000493919.5:c.941C= ENSP00000418819.1:p.Pro314=
ENST00000586385.5:c.5-12630C= ENSP00000465818.1:n.5-12630C=
ENST00000591534.5:c.-43-2060C= ENSP00000467329.1:n.-43-2060C=
ENST00000591849.5:c.-98-26391C= ENSP00000465347.1:n.-98-26391C=
ENST00000621897.1:n.282C=
NM_007294.3:c.4391C= , LRG_292t1:c.4391C= NP_009225.1:p.Pro1464=
NM_007297.3:c.4250C= NP_009228.2:p.Pro1417=
NM_007298.3:c.1079C= NP_009229.2:p.Pro360=
NM_007299.3:c.1079C= NP_009230.2:p.Pro360=
NM_007300.3:c.4454C= NP_009231.2:p.Pro1485=
NR_027676.1:n.4527C=
NM_007294.4:c.4391C= MANE Select NP_009225.1:p.Pro1464=
NM_007297.4:c.4250C= NP_009228.2:p.Pro1417=
NM_007299.4:c.1079C= NP_009230.2:p.Pro360=
NM_007300.4:c.4454C= NP_009231.2:p.Pro1485=
NR_027676.2:n.4568C=