Canonical Allele Identifier: CA1327046392
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214730462C= , CM000664.2:g.214730462C= GRCh38
NC_000002.11:g.215595186C= , CM000664.1:g.215595186C= GRCh37
NC_000002.10:g.215303431C= NCBI36
NG_012047.2:g.84243G=
NG_012047.3:g.84250G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1950G= MANE Select ENSP00000260947.4:p.Lys650=
ENST00000421162.2:c.597G= ENSP00000392245.2:p.Lys199=
ENST00000613192.2:c.*13G= ENSP00000483275.2:n.*13G=
ENST00000613374.5:c.540G= ENSP00000484464.1:p.Lys180=
ENST00000613706.5:c.1542G= ENSP00000484976.2:p.Lys514=
ENST00000617164.5:c.1893G= ENSP00000480470.1:p.Lys631=
ENST00000619009.5:c.411G= ENSP00000482293.1:p.Lys137=
ENST00000650978.1:c.3325G=
ENST00000260947.8:c.1950G= ENSP00000260947.4:p.Lys650=
ENST00000421162.1:c.597G= ENSP00000392245.1:p.Lys199=
ENST00000432456.5:c.47G=
ENST00000455743.5:c.*1570G= ENSP00000412186.1:n.*1570G=
ENST00000471590.5:n.285G=
ENST00000613192.1:c.120G= ENSP00000483275.1:p.Lys40=
ENST00000613374.4:c.540G= ENSP00000484464.1:p.Lys180=
ENST00000613706.4:c.597G= ENSP00000484976.1:p.Lys199=
ENST00000617164.4:c.1893G= ENSP00000480470.1:p.Lys631=
ENST00000619009.4:c.411G= ENSP00000482293.1:p.Lys137=
ENST00000620057.4:c.*616G= ENSP00000481988.1:n.*616G=
NM_000465.3:c.1950G= NP_000456.2:p.Lys650=
NM_001282543.1:c.1893G= NP_001269472.1:p.Lys631=
NM_001282545.1:c.597G= NP_001269474.1:p.Lys199=
NM_001282548.1:c.540G= NP_001269477.1:p.Lys180=
NM_001282549.1:c.411G= NP_001269478.1:p.Lys137=
NR_104212.1:n.1943G=
NR_104215.1:n.1886G=
NR_104216.1:n.1142G=
XM_011511567.1:c.1896G= XP_011509869.1:p.Lys632=
XM_017004613.1:c.2049G= XP_016860102.1:p.Lys683=
XR_002959322.1:n.2140G=
NM_000465.4:c.1950G= MANE Select NP_000456.2:p.Lys650=
NM_001282543.2:c.1893G= NP_001269472.1:p.Lys631=
NM_001282545.2:c.597G= NP_001269474.1:p.Lys199=
NM_001282548.2:c.540G= NP_001269477.1:p.Lys180=
NM_001282549.2:c.411G= NP_001269478.1:p.Lys137=
NR_104212.2:n.1915G=
NR_104215.2:n.1858G=
NR_104216.2:n.1114G=