Canonical Allele Identifier: CA350449734
Gene: BARD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728699C>A , CM000664.2:g.214728699C>A GRCh38
NC_000002.11:g.215593423C>A , CM000664.1:g.215593423C>A GRCh37
NC_000002.10:g.215301668C>A NCBI36
NG_012047.2:g.86006G>T
NG_012047.3:g.86013G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.2311G>T MANE Select ENSP00000260947.4:p.Glu771Ter
ENST00000421162.2:c.958G>T ENSP00000392245.2:p.Glu320Ter
ENST00000613192.2:c.*374G>T ENSP00000483275.2:n.*374G>T
ENST00000613374.5:c.901G>T ENSP00000484464.1:p.Glu301Ter
ENST00000613706.5:c.1903G>T ENSP00000484976.2:p.Glu635Ter
ENST00000617164.5:c.2254G>T ENSP00000480470.1:p.Glu752Ter
ENST00000619009.5:c.772G>T ENSP00000482293.1:p.Glu258Ter
ENST00000650978.1:c.3686G>T
ENST00000260947.8:c.2311G>T ENSP00000260947.4:p.Glu771Ter
ENST00000432456.5:c.454G>T
ENST00000471590.5:n.646G>T
ENST00000613192.1:c.481G>T ENSP00000483275.1:p.Glu161Ter
ENST00000613374.4:c.901G>T ENSP00000484464.1:p.Glu301Ter
ENST00000613706.4:c.958G>T ENSP00000484976.1:p.Glu320Ter
ENST00000617164.4:c.2254G>T ENSP00000480470.1:p.Glu752Ter
ENST00000619009.4:c.772G>T ENSP00000482293.1:p.Glu258Ter
ENST00000620057.4:c.*977G>T ENSP00000481988.1:n.*977G>T
NM_000465.3:c.2311G>T NP_000456.2:p.Glu771Ter
NM_001282543.1:c.2254G>T NP_001269472.1:p.Glu752Ter
NM_001282545.1:c.958G>T NP_001269474.1:p.Glu320Ter
NM_001282548.1:c.901G>T NP_001269477.1:p.Glu301Ter
NM_001282549.1:c.772G>T NP_001269478.1:p.Glu258Ter
NR_104212.1:n.2304G>T
NR_104215.1:n.2247G>T
NR_104216.1:n.1503G>T
XM_011511567.1:c.2257G>T XP_011509869.1:p.Glu753Ter
XM_017004613.1:c.2410G>T XP_016860102.1:p.Glu804Ter
XR_002959322.1:n.2677G>T
NM_000465.4:c.2311G>T MANE Select NP_000456.2:p.Glu771Ter
NM_001282543.2:c.2254G>T NP_001269472.1:p.Glu752Ter
NM_001282545.2:c.958G>T NP_001269474.1:p.Glu320Ter
NM_001282548.2:c.901G>T NP_001269477.1:p.Glu301Ter
NM_001282549.2:c.772G>T NP_001269478.1:p.Glu258Ter
NR_104212.2:n.2276G>T
NR_104215.2:n.2219G>T
NR_104216.2:n.1475G>T