Canonical Allele Identifier: CA1327046380
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214730451G= , CM000664.2:g.214730451G= GRCh38
NC_000002.11:g.215595175G= , CM000664.1:g.215595175G= GRCh37
NC_000002.10:g.215303420G= NCBI36
NG_012047.2:g.84254C=
NG_012047.3:g.84261C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1961C= MANE Select ENSP00000260947.4:p.Pro654=
ENST00000421162.2:c.608C= ENSP00000392245.2:p.Pro203=
ENST00000613192.2:c.*24C= ENSP00000483275.2:n.*24C=
ENST00000613374.5:c.551C= ENSP00000484464.1:p.Pro184=
ENST00000613706.5:c.1553C= ENSP00000484976.2:p.Pro518=
ENST00000617164.5:c.1904C= ENSP00000480470.1:p.Pro635=
ENST00000619009.5:c.422C= ENSP00000482293.1:p.Pro141=
ENST00000650978.1:c.3336C=
ENST00000260947.8:c.1961C= ENSP00000260947.4:p.Pro654=
ENST00000421162.1:c.608C= ENSP00000392245.1:p.Pro203=
ENST00000432456.5:c.58C=
ENST00000455743.5:c.*1581C= ENSP00000412186.1:n.*1581C=
ENST00000471590.5:n.296C=
ENST00000613192.1:c.131C= ENSP00000483275.1:p.Pro44=
ENST00000613374.4:c.551C= ENSP00000484464.1:p.Pro184=
ENST00000613706.4:c.608C= ENSP00000484976.1:p.Pro203=
ENST00000617164.4:c.1904C= ENSP00000480470.1:p.Pro635=
ENST00000619009.4:c.422C= ENSP00000482293.1:p.Pro141=
ENST00000620057.4:c.*627C= ENSP00000481988.1:n.*627C=
NM_000465.3:c.1961C= NP_000456.2:p.Pro654=
NM_001282543.1:c.1904C= NP_001269472.1:p.Pro635=
NM_001282545.1:c.608C= NP_001269474.1:p.Pro203=
NM_001282548.1:c.551C= NP_001269477.1:p.Pro184=
NM_001282549.1:c.422C= NP_001269478.1:p.Pro141=
NR_104212.1:n.1954C=
NR_104215.1:n.1897C=
NR_104216.1:n.1153C=
XM_011511567.1:c.1907C= XP_011509869.1:p.Pro636=
XM_017004613.1:c.2060C= XP_016860102.1:p.Pro687=
XR_002959322.1:n.2151C=
NM_000465.4:c.1961C= MANE Select NP_000456.2:p.Pro654=
NM_001282543.2:c.1904C= NP_001269472.1:p.Pro635=
NM_001282545.2:c.608C= NP_001269474.1:p.Pro203=
NM_001282548.2:c.551C= NP_001269477.1:p.Pro184=
NM_001282549.2:c.422C= NP_001269478.1:p.Pro141=
NR_104212.2:n.1926C=
NR_104215.2:n.1869C=
NR_104216.2:n.1125C=