Canonical Allele Identifier: CA539837372
Gene: BARD1 HGNC NCBI

Linked Data

dbSNP Id: rs1222686156

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214792250G>C , CM000664.2:g.214792250G>C GRCh38
NC_000002.11:g.215656974G>C , CM000664.1:g.215656974G>C GRCh37
NC_000002.10:g.215365219G>C NCBI36
NG_012047.2:g.22455C>G
NG_012047.3:g.22462C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.364+47C>G MANE Select ENSP00000260947.4:n.364+47C>G
ENST00000421162.2:c.215+4811C>G ENSP00000392245.2:n.215+4811C>G
ENST00000613192.2:c.158+17162C>G ENSP00000483275.2:n.158+17162C>G
ENST00000613374.5:c.158+17162C>G ENSP00000484464.1:n.158+17162C>G
ENST00000613706.5:c.364+47C>G ENSP00000484976.2:n.364+47C>G
ENST00000617164.5:c.307+47C>G ENSP00000480470.1:n.307+47C>G
ENST00000619009.5:c.364+47C>G ENSP00000482293.1:n.364+47C>G
ENST00000650978.1:c.206+47C>G
ENST00000260947.8:c.364+47C>G ENSP00000260947.4:n.364+47C>G
ENST00000421162.1:c.215+4811C>G ENSP00000392245.1:n.215+4811C>G
ENST00000455743.5:c.215+4811C>G ENSP00000412186.1:n.215+4811C>G
ENST00000471787.1:n.260-10741C>G
ENST00000613192.1:c.73+17162C>G ENSP00000483275.1:n.73+17162C>G
ENST00000613374.4:c.158+17162C>G ENSP00000484464.1:n.158+17162C>G
ENST00000613706.4:c.215+4811C>G ENSP00000484976.1:n.215+4811C>G
ENST00000617164.4:c.307+47C>G ENSP00000480470.1:n.307+47C>G
ENST00000619009.4:c.364+47C>G ENSP00000482293.1:n.364+47C>G
ENST00000620057.4:c.364+47C>G ENSP00000481988.1:n.364+47C>G
NM_000465.3:c.364+47C>G NP_000456.2:n.364+47C>G
NM_001282543.1:c.307+47C>G NP_001269472.1:n.307+47C>G
NM_001282545.1:c.215+4811C>G NP_001269474.1:n.215+4811C>G
NM_001282548.1:c.158+17162C>G NP_001269477.1:n.158+17162C>G
NM_001282549.1:c.364+47C>G NP_001269478.1:n.364+47C>G
NR_104212.1:n.357+4811C>G
NR_104215.1:n.301-10741C>G
NR_104216.1:n.506+47C>G
XM_011511567.1:c.310+47C>G XP_011509869.1:n.310+47C>G
XM_011511568.1:c.364+47C>G XP_011509870.1:n.364+47C>G
XM_017004613.1:c.463+47C>G XP_016860102.1:n.463+47C>G
XM_017004614.1:c.463+47C>G XP_016860103.1:n.463+47C>G
XR_002959322.1:n.554+47C>G
NM_000465.4:c.364+47C>G MANE Select NP_000456.2:n.364+47C>G
NM_001282543.2:c.307+47C>G NP_001269472.1:n.307+47C>G
NM_001282545.2:c.215+4811C>G NP_001269474.1:n.215+4811C>G
NM_001282548.2:c.158+17162C>G NP_001269477.1:n.158+17162C>G
NM_001282549.2:c.364+47C>G NP_001269478.1:n.364+47C>G
NR_104212.2:n.329+4811C>G
NR_104215.2:n.273-10741C>G
NR_104216.2:n.478+47C>G