Canonical Allele Identifier: CA431135822
Gene: BARD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215646103G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214781379G>T , CM000664.2:g.214781379G>T GRCh38
NC_000002.11:g.215646103G>T , CM000664.1:g.215646103G>T GRCh37
NC_000002.10:g.215354348G>T NCBI36
NG_012047.2:g.33326C>A
NG_012047.3:g.33333C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.495C>A MANE Select ENSP00000260947.4:p.Thr165=
ENST00000421162.2:c.215+15682C>A ENSP00000392245.2:n.215+15682C>A
ENST00000613192.2:c.158+28033C>A ENSP00000483275.2:n.158+28033C>A
ENST00000613374.5:c.158+28033C>A ENSP00000484464.1:n.158+28033C>A
ENST00000613706.5:c.495C>A ENSP00000484976.2:p.Thr165=
ENST00000617164.5:c.438C>A ENSP00000480470.1:p.Thr146=
ENST00000619009.5:c.364+10918C>A ENSP00000482293.1:n.364+10918C>A
ENST00000650978.1:c.337C>A
ENST00000260947.8:c.495C>A ENSP00000260947.4:p.Thr165=
ENST00000421162.1:c.215+15682C>A ENSP00000392245.1:n.215+15682C>A
ENST00000455743.5:c.*115C>A ENSP00000412186.1:n.*115C>A
ENST00000471787.1:n.390C>A
ENST00000613192.1:c.73+28033C>A ENSP00000483275.1:n.73+28033C>A
ENST00000613374.4:c.158+28033C>A ENSP00000484464.1:n.158+28033C>A
ENST00000613706.4:c.215+15682C>A ENSP00000484976.1:n.215+15682C>A
ENST00000617164.4:c.438C>A ENSP00000480470.1:p.Thr146=
ENST00000619009.4:c.364+10918C>A ENSP00000482293.1:n.364+10918C>A
ENST00000620057.4:c.364+10918C>A ENSP00000481988.1:n.364+10918C>A
NM_000465.3:c.495C>A NP_000456.2:p.Thr165=
NM_001282543.1:c.438C>A NP_001269472.1:p.Thr146=
NM_001282545.1:c.215+15682C>A NP_001269474.1:n.215+15682C>A
NM_001282548.1:c.158+28033C>A NP_001269477.1:n.158+28033C>A
NM_001282549.1:c.364+10918C>A NP_001269478.1:n.364+10918C>A
NR_104212.1:n.488C>A
NR_104215.1:n.431C>A
NR_104216.1:n.506+10918C>A
XM_011511567.1:c.441C>A XP_011509869.1:p.Thr147=
XM_011511568.1:c.495C>A XP_011509870.1:p.Thr165=
XM_017004613.1:c.594C>A XP_016860102.1:p.Thr198=
XM_017004614.1:c.594C>A XP_016860103.1:p.Thr198=
XR_002959322.1:n.685C>A
NM_000465.4:c.495C>A MANE Select NP_000456.2:p.Thr165=
NM_001282543.2:c.438C>A NP_001269472.1:p.Thr146=
NM_001282545.2:c.215+15682C>A NP_001269474.1:n.215+15682C>A
NM_001282548.2:c.158+28033C>A NP_001269477.1:n.158+28033C>A
NM_001282549.2:c.364+10918C>A NP_001269478.1:n.364+10918C>A
NR_104212.2:n.460C>A
NR_104215.2:n.403C>A
NR_104216.2:n.478+10918C>A