Canonical Allele Identifier: CA2260766384
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43057072T= , CM000679.2:g.43057072T= GRCh38
NC_000017.10:g.41209089T= , CM000679.1:g.41209089T= GRCh37
NC_000017.9:g.38462615T= NCBI36
NG_005905.2:g.160912A= , LRG_292:g.160912A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5254A= ENSP00000417241.2:p.Arg1752=
ENST00000470026.6:c.5257A= ENSP00000419274.2:p.Arg1753=
ENST00000473961.6:c.5131A= ENSP00000420201.2:p.Arg1711=
ENST00000476777.6:c.5251A= ENSP00000417554.2:p.Arg1751=
ENST00000477152.6:c.5179A= ENSP00000419988.2:p.Arg1727=
ENST00000478531.6:c.1945A= ENSP00000420412.2:p.Arg649=
ENST00000489037.2:c.5179A= ENSP00000420781.2:p.Arg1727=
ENST00000493919.6:c.1807A= ENSP00000418819.2:p.Arg603=
ENST00000494123.6:c.5257A= ENSP00000419103.2:p.Arg1753=
ENST00000497488.2:c.4369A= ENSP00000418986.2:p.Arg1457=
ENST00000618469.2:c.5257A= ENSP00000478114.2:p.Arg1753=
ENST00000634433.2:c.5134A= ENSP00000489431.2:p.Arg1712=
ENST00000644379.2:c.5323A= ENSP00000496570.2:p.Arg1775=
ENST00000644555.2:c.1807A= ENSP00000494614.2:p.Arg603=
ENST00000652672.2:c.5116A= ENSP00000498906.2:p.Arg1706=
ENST00000484087.6:c.1819A= ENSP00000419481.2:p.Arg607=
ENST00000357654.9:c.5257A= MANE Select ENSP00000350283.3:p.Arg1753=
ENST00000471181.7:c.5320A= ENSP00000418960.2:p.Arg1774=
ENST00000644379.1:c.1644A=
ENST00000352993.7:c.1831A= ENSP00000312236.5:p.Arg611=
ENST00000357654.7:c.5257A= ENSP00000350283.3:p.Arg1753=
ENST00000461221.5:c.*5040A= ENSP00000418548.1:n.*5040A=
ENST00000468300.5:c.1945A= ENSP00000417148.1:p.Arg649=
ENST00000471181.6:c.5320A= ENSP00000418960.2:p.Arg1774=
ENST00000491747.6:c.1945A= ENSP00000420705.2:p.Arg649=
ENST00000493795.5:c.5116A= ENSP00000418775.1:p.Arg1706=
ENST00000586385.5:c.187A= ENSP00000465818.1:p.Arg63=
ENST00000591534.5:c.730A= ENSP00000467329.1:p.Arg244=
ENST00000591849.5:c.-98-6882A= ENSP00000465347.1:n.-98-6882A=
NM_007294.3:c.5257A= , LRG_292t1:c.5257A= NP_009225.1:p.Arg1753=
NM_007297.3:c.5116A= NP_009228.2:p.Arg1706=
NM_007298.3:c.1945A= NP_009229.2:p.Arg649=
NM_007299.3:c.1945A= NP_009230.2:p.Arg649=
NM_007300.3:c.5320A= NP_009231.2:p.Arg1774=
NR_027676.1:n.5393A=
NM_007294.4:c.5257A= MANE Select NP_009225.1:p.Arg1753=
NM_007297.4:c.5116A= NP_009228.2:p.Arg1706=
NM_007299.4:c.1945A= NP_009230.2:p.Arg649=
NM_007300.4:c.5320A= NP_009231.2:p.Arg1774=
NR_027676.2:n.5434A=