Canonical Allele Identifier: CA2260762791
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43049188A= , CM000679.2:g.43049188A= GRCh38
NC_000017.10:g.41201205A= , CM000679.1:g.41201205A= GRCh37
NC_000017.9:g.38454731A= NCBI36
NG_005905.2:g.168796T= , LRG_292:g.168796T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5336T= ENSP00000417241.2:p.Leu1779=
ENST00000470026.6:c.5339T= ENSP00000419274.2:p.Leu1780=
ENST00000473961.6:c.5213T= ENSP00000420201.2:p.Leu1738=
ENST00000476777.6:c.5333T= ENSP00000417554.2:p.Leu1778=
ENST00000477152.6:c.5261T= ENSP00000419988.2:p.Leu1754=
ENST00000478531.6:c.2027T= ENSP00000420412.2:p.Leu676=
ENST00000489037.2:c.5261T= ENSP00000420781.2:p.Leu1754=
ENST00000493919.6:c.1889T= ENSP00000418819.2:p.Leu630=
ENST00000494123.6:c.5339T= ENSP00000419103.2:p.Leu1780=
ENST00000497488.2:c.4451T= ENSP00000418986.2:p.Leu1484=
ENST00000618469.2:c.5339T= ENSP00000478114.2:p.Leu1780=
ENST00000634433.2:c.5216T= ENSP00000489431.2:p.Leu1739=
ENST00000644379.2:c.5405T= ENSP00000496570.2:p.Leu1802=
ENST00000644555.2:c.1889T= ENSP00000494614.2:p.Leu630=
ENST00000652672.2:c.5198T= ENSP00000498906.2:p.Leu1733=
ENST00000484087.6:c.1901T= ENSP00000419481.2:p.Leu634=
ENST00000700081.1:n.1222T=
ENST00000357654.9:c.5339T= MANE Select ENSP00000350283.3:p.Leu1780=
ENST00000471181.7:c.5402T= ENSP00000418960.2:p.Leu1801=
ENST00000644379.1:c.1726T=
ENST00000352993.7:c.1913T= ENSP00000312236.5:p.Leu638=
ENST00000357654.7:c.5339T= ENSP00000350283.3:p.Leu1780=
ENST00000461221.5:c.*5122T= ENSP00000418548.1:n.*5122T=
ENST00000468300.5:c.2021-1485T= ENSP00000417148.1:n.2021-1485T=
ENST00000471181.6:c.5402T= ENSP00000418960.2:p.Leu1801=
ENST00000491747.6:c.2027T= ENSP00000420705.2:p.Leu676=
ENST00000493795.5:c.5198T= ENSP00000418775.1:p.Leu1733=
ENST00000586385.5:c.269T= ENSP00000465818.1:p.Leu90=
ENST00000591534.5:c.812T= ENSP00000467329.1:p.Leu271=
ENST00000591849.5:c.38T= ENSP00000465347.1:p.Leu13=
NM_007294.3:c.5339T= , LRG_292t1:c.5339T= NP_009225.1:p.Leu1780=
NM_007297.3:c.5198T= NP_009228.2:p.Leu1733=
NM_007298.3:c.2027T= NP_009229.2:p.Leu676=
NM_007299.3:c.2021-1485T= NP_009230.2:n.2021-1485T=
NM_007300.3:c.5402T= NP_009231.2:p.Leu1801=
NR_027676.1:n.5475T=
NM_007294.4:c.5339T= MANE Select NP_009225.1:p.Leu1780=
NM_007297.4:c.5198T= NP_009228.2:p.Leu1733=
NM_007299.4:c.2021-1485T= NP_009230.2:n.2021-1485T=
NM_007300.4:c.5402T= NP_009231.2:p.Leu1801=
NR_027676.2:n.5516T=