Canonical Allele Identifier: CA2260775550
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43076603A= , CM000679.2:g.43076603A= GRCh38
NC_000017.10:g.41228620A= , CM000679.1:g.41228620A= GRCh37
NC_000017.9:g.38482146A= NCBI36
NG_005905.2:g.141381T= , LRG_292:g.141381T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4366T= ENSP00000417241.2:p.Ser1456=
ENST00000470026.6:c.4369T= ENSP00000419274.2:p.Ser1457=
ENST00000473961.6:c.4243T= ENSP00000420201.2:p.Ser1415=
ENST00000476777.6:c.4363T= ENSP00000417554.2:p.Ser1455=
ENST00000477152.6:c.4291T= ENSP00000419988.2:p.Ser1431=
ENST00000478531.6:c.1057T= ENSP00000420412.2:p.Ser353=
ENST00000489037.2:c.4291T= ENSP00000420781.2:p.Ser1431=
ENST00000493919.6:c.919T= ENSP00000418819.2:p.Ser307=
ENST00000494123.6:c.4369T= ENSP00000419103.2:p.Ser1457=
ENST00000497488.2:c.3481T= ENSP00000418986.2:p.Ser1161=
ENST00000618469.2:c.4369T= ENSP00000478114.2:p.Ser1457=
ENST00000634433.2:c.4246T= ENSP00000489431.2:p.Ser1416=
ENST00000644379.2:c.4435T= ENSP00000496570.2:p.Ser1479=
ENST00000644555.2:c.919T= ENSP00000494614.2:p.Ser307=
ENST00000652672.2:c.4228T= ENSP00000498906.2:p.Ser1410=
ENST00000484087.6:c.931T= ENSP00000419481.2:p.Ser311=
ENST00000700182.1:c.976T= ENSP00000514849.1:p.Ser326=
ENST00000357654.9:c.4369T= MANE Select ENSP00000350283.3:p.Ser1457=
ENST00000471181.7:c.4432T= ENSP00000418960.2:p.Ser1478=
ENST00000644379.1:c.756T=
ENST00000352993.7:c.943T= ENSP00000312236.5:p.Ser315=
ENST00000357654.7:c.4369T= ENSP00000350283.3:p.Ser1457=
ENST00000461221.5:c.*4152T= ENSP00000418548.1:n.*4152T=
ENST00000461574.1:c.660T=
ENST00000468300.5:c.1057T= ENSP00000417148.1:p.Ser353=
ENST00000471181.6:c.4432T= ENSP00000418960.2:p.Ser1478=
ENST00000478531.5:c.1057T= ENSP00000420412.1:p.Ser353=
ENST00000484087.5:c.682T= ENSP00000419481.1:p.Ser228=
ENST00000487825.5:c.685T= ENSP00000418212.1:p.Ser229=
ENST00000491747.6:c.1057T= ENSP00000420705.2:p.Ser353=
ENST00000493795.5:c.4228T= ENSP00000418775.1:p.Ser1410=
ENST00000493919.5:c.919T= ENSP00000418819.1:p.Ser307=
ENST00000586385.5:c.5-12652T= ENSP00000465818.1:n.5-12652T=
ENST00000591534.5:c.-43-2082T= ENSP00000467329.1:n.-43-2082T=
ENST00000591849.5:c.-98-26413T= ENSP00000465347.1:n.-98-26413T=
ENST00000621897.1:n.260T=
NM_007294.3:c.4369T= , LRG_292t1:c.4369T= NP_009225.1:p.Ser1457=
NM_007297.3:c.4228T= NP_009228.2:p.Ser1410=
NM_007298.3:c.1057T= NP_009229.2:p.Ser353=
NM_007299.3:c.1057T= NP_009230.2:p.Ser353=
NM_007300.3:c.4432T= NP_009231.2:p.Ser1478=
NR_027676.1:n.4505T=
NM_007294.4:c.4369T= MANE Select NP_009225.1:p.Ser1457=
NM_007297.4:c.4228T= NP_009228.2:p.Ser1410=
NM_007299.4:c.1057T= NP_009230.2:p.Ser353=
NM_007300.4:c.4432T= NP_009231.2:p.Ser1478=
NR_027676.2:n.4546T=