Canonical Allele Identifier: CA2260766476
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43057134T= , CM000679.2:g.43057134T= GRCh38
NC_000017.10:g.41209151T= , CM000679.1:g.41209151T= GRCh37
NC_000017.9:g.38462677T= NCBI36
NG_005905.2:g.160850A= , LRG_292:g.160850A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5192A= ENSP00000417241.2:p.His1731=
ENST00000470026.6:c.5195A= ENSP00000419274.2:p.His1732=
ENST00000473961.6:c.5069A= ENSP00000420201.2:p.His1690=
ENST00000476777.6:c.5189A= ENSP00000417554.2:p.His1730=
ENST00000477152.6:c.5117A= ENSP00000419988.2:p.His1706=
ENST00000478531.6:c.1883A= ENSP00000420412.2:p.His628=
ENST00000489037.2:c.5117A= ENSP00000420781.2:p.His1706=
ENST00000493919.6:c.1745A= ENSP00000418819.2:p.His582=
ENST00000494123.6:c.5195A= ENSP00000419103.2:p.His1732=
ENST00000497488.2:c.4307A= ENSP00000418986.2:p.His1436=
ENST00000618469.2:c.5195A= ENSP00000478114.2:p.His1732=
ENST00000634433.2:c.5072A= ENSP00000489431.2:p.His1691=
ENST00000644379.2:c.5261A= ENSP00000496570.2:p.His1754=
ENST00000644555.2:c.1745A= ENSP00000494614.2:p.His582=
ENST00000652672.2:c.5054A= ENSP00000498906.2:p.His1685=
ENST00000484087.6:c.1757A= ENSP00000419481.2:p.His586=
ENST00000357654.9:c.5195A= MANE Select ENSP00000350283.3:p.His1732=
ENST00000471181.7:c.5258A= ENSP00000418960.2:p.His1753=
ENST00000644379.1:c.1582A=
ENST00000352993.7:c.1769A= ENSP00000312236.5:p.His590=
ENST00000357654.7:c.5195A= ENSP00000350283.3:p.His1732=
ENST00000461221.5:c.*4978A= ENSP00000418548.1:n.*4978A=
ENST00000468300.5:c.1883A= ENSP00000417148.1:p.His628=
ENST00000471181.6:c.5258A= ENSP00000418960.2:p.His1753=
ENST00000491747.6:c.1883A= ENSP00000420705.2:p.His628=
ENST00000493795.5:c.5054A= ENSP00000418775.1:p.His1685=
ENST00000586385.5:c.125A= ENSP00000465818.1:p.His42=
ENST00000591534.5:c.668A= ENSP00000467329.1:p.His223=
ENST00000591849.5:c.-98-6944A= ENSP00000465347.1:n.-98-6944A=
NM_007294.3:c.5195A= , LRG_292t1:c.5195A= NP_009225.1:p.His1732=
NM_007297.3:c.5054A= NP_009228.2:p.His1685=
NM_007298.3:c.1883A= NP_009229.2:p.His628=
NM_007299.3:c.1883A= NP_009230.2:p.His628=
NM_007300.3:c.5258A= NP_009231.2:p.His1753=
NR_027676.1:n.5331A=
NM_007294.4:c.5195A= MANE Select NP_009225.1:p.His1732=
NM_007297.4:c.5054A= NP_009228.2:p.His1685=
NM_007299.4:c.1883A= NP_009230.2:p.His628=
NM_007300.4:c.5258A= NP_009231.2:p.His1753=
NR_027676.2:n.5372A=