Canonical Allele Identifier: CA350449671
Gene: BARD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728689G>T , CM000664.2:g.214728689G>T GRCh38
NC_000002.11:g.215593413G>T , CM000664.1:g.215593413G>T GRCh37
NC_000002.10:g.215301658G>T NCBI36
NG_012047.2:g.86016C>A
NG_012047.3:g.86023C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.2321C>A MANE Select ENSP00000260947.4:p.Pro774His
ENST00000421162.2:c.968C>A ENSP00000392245.2:p.Pro323His
ENST00000613192.2:c.*384C>A ENSP00000483275.2:n.*384C>A
ENST00000613374.5:c.911C>A ENSP00000484464.1:p.Pro304His
ENST00000613706.5:c.1913C>A ENSP00000484976.2:p.Pro638His
ENST00000617164.5:c.2264C>A ENSP00000480470.1:p.Pro755His
ENST00000619009.5:c.782C>A ENSP00000482293.1:p.Pro261His
ENST00000650978.1:c.3696C>A
ENST00000260947.8:c.2321C>A ENSP00000260947.4:p.Pro774His
ENST00000432456.5:c.464C>A
ENST00000471590.5:n.656C>A
ENST00000613192.1:c.491C>A ENSP00000483275.1:p.Pro164His
ENST00000613374.4:c.911C>A ENSP00000484464.1:p.Pro304His
ENST00000613706.4:c.968C>A ENSP00000484976.1:p.Pro323His
ENST00000617164.4:c.2264C>A ENSP00000480470.1:p.Pro755His
ENST00000619009.4:c.782C>A ENSP00000482293.1:p.Pro261His
ENST00000620057.4:c.*987C>A ENSP00000481988.1:n.*987C>A
NM_000465.3:c.2321C>A NP_000456.2:p.Pro774His
NM_001282543.1:c.2264C>A NP_001269472.1:p.Pro755His
NM_001282545.1:c.968C>A NP_001269474.1:p.Pro323His
NM_001282548.1:c.911C>A NP_001269477.1:p.Pro304His
NM_001282549.1:c.782C>A NP_001269478.1:p.Pro261His
NR_104212.1:n.2314C>A
NR_104215.1:n.2257C>A
NR_104216.1:n.1513C>A
XM_011511567.1:c.2267C>A XP_011509869.1:p.Pro756His
XM_017004613.1:c.2420C>A XP_016860102.1:p.Pro807His
XR_002959322.1:n.2687C>A
NM_000465.4:c.2321C>A MANE Select NP_000456.2:p.Pro774His
NM_001282543.2:c.2264C>A NP_001269472.1:p.Pro755His
NM_001282545.2:c.968C>A NP_001269474.1:p.Pro323His
NM_001282548.2:c.911C>A NP_001269477.1:p.Pro304His
NM_001282549.2:c.782C>A NP_001269478.1:p.Pro261His
NR_104212.2:n.2286C>A
NR_104215.2:n.2229C>A
NR_104216.2:n.1485C>A