Canonical Allele Identifier: CA431391074
Gene: BARD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.215645647T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214780923T>C , CM000664.2:g.214780923T>C GRCh38
NC_000002.11:g.215645647T>C , CM000664.1:g.215645647T>C GRCh37
NC_000002.10:g.215353892T>C NCBI36
NG_012047.2:g.33782A>G
NG_012047.3:g.33789A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.951A>G MANE Select ENSP00000260947.4:p.Glu317=
ENST00000421162.2:c.215+16138A>G ENSP00000392245.2:n.215+16138A>G
ENST00000613192.2:c.158+28489A>G ENSP00000483275.2:n.158+28489A>G
ENST00000613374.5:c.159-28368A>G ENSP00000484464.1:n.159-28368A>G
ENST00000613706.5:c.906+45A>G ENSP00000484976.2:n.906+45A>G
ENST00000617164.5:c.894A>G ENSP00000480470.1:p.Glu298=
ENST00000619009.5:c.364+11374A>G ENSP00000482293.1:n.364+11374A>G
ENST00000650978.1:c.793A>G
ENST00000260947.8:c.951A>G ENSP00000260947.4:p.Glu317=
ENST00000421162.1:c.215+16138A>G ENSP00000392245.1:n.215+16138A>G
ENST00000455743.5:c.*571A>G ENSP00000412186.1:n.*571A>G
ENST00000471787.1:n.846A>G
ENST00000613192.1:c.73+28489A>G ENSP00000483275.1:n.73+28489A>G
ENST00000613374.4:c.159-28368A>G ENSP00000484464.1:n.159-28368A>G
ENST00000613706.4:c.215+16138A>G ENSP00000484976.1:n.215+16138A>G
ENST00000617164.4:c.894A>G ENSP00000480470.1:p.Glu298=
ENST00000619009.4:c.364+11374A>G ENSP00000482293.1:n.364+11374A>G
ENST00000620057.4:c.364+11374A>G ENSP00000481988.1:n.364+11374A>G
NM_000465.3:c.951A>G NP_000456.2:p.Glu317=
NM_001282543.1:c.894A>G NP_001269472.1:p.Glu298=
NM_001282545.1:c.215+16138A>G NP_001269474.1:n.215+16138A>G
NM_001282548.1:c.159-28368A>G NP_001269477.1:n.159-28368A>G
NM_001282549.1:c.364+11374A>G NP_001269478.1:n.364+11374A>G
NR_104212.1:n.944A>G
NR_104215.1:n.887A>G
NR_104216.1:n.506+11374A>G
XM_011511567.1:c.897A>G XP_011509869.1:p.Glu299=
XM_011511568.1:c.951A>G XP_011509870.1:p.Glu317=
XM_017004613.1:c.1050A>G XP_016860102.1:p.Glu350=
XM_017004614.1:c.1050A>G XP_016860103.1:p.Glu350=
XR_002959322.1:n.1141A>G
NM_000465.4:c.951A>G MANE Select NP_000456.2:p.Glu317=
NM_001282543.2:c.894A>G NP_001269472.1:p.Glu298=
NM_001282545.2:c.215+16138A>G NP_001269474.1:n.215+16138A>G
NM_001282548.2:c.159-28368A>G NP_001269477.1:n.159-28368A>G
NM_001282549.2:c.364+11374A>G NP_001269478.1:n.364+11374A>G
NR_104212.2:n.916A>G
NR_104215.2:n.859A>G
NR_104216.2:n.478+11374A>G