Canonical Allele Identifier: CA1327045489
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728747_214728749delinsCTT , CM000664.2:g.214728747_214728749delinsCTT GRCh38
NC_000002.11:g.215593471_215593473delinsCTT , CM000664.1:g.215593471_215593473delinsCTT GRCh37
NC_000002.10:g.215301716_215301718delinsCTT NCBI36
NG_012047.2:g.85956_85958delinsAAG
NG_012047.3:g.85963_85965delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.2261_2263delinsAAG MANE Select ENSP00000260947.4:p.Lys754=
ENST00000421162.2:c.908_910delinsAAG ENSP00000392245.2:p.Lys303=
ENST00000613192.2:c.*324_*326delinsAAG ENSP00000483275.2:n.*324_*326delinsAAG
ENST00000613374.5:c.851_853delinsAAG ENSP00000484464.1:p.Lys284=
ENST00000613706.5:c.1853_1855delinsAAG ENSP00000484976.2:p.Lys618=
ENST00000617164.5:c.2204_2206delinsAAG ENSP00000480470.1:p.Lys735=
ENST00000619009.5:c.722_724delinsAAG ENSP00000482293.1:p.Lys241=
ENST00000650978.1:c.3636_3638delinsAAG
ENST00000260947.8:c.2261_2263delinsAAG ENSP00000260947.4:p.Lys754=
ENST00000432456.5:c.404_406delinsAAG
ENST00000455743.5:c.*1881_*1883delinsAAG ENSP00000412186.1:n.*1881_*1883delinsAAG
ENST00000471590.5:n.596_598delinsAAG
ENST00000613192.1:c.431_433delinsAAG ENSP00000483275.1:p.Lys144=
ENST00000613374.4:c.851_853delinsAAG ENSP00000484464.1:p.Lys284=
ENST00000613706.4:c.908_910delinsAAG ENSP00000484976.1:p.Lys303=
ENST00000617164.4:c.2204_2206delinsAAG ENSP00000480470.1:p.Lys735=
ENST00000619009.4:c.722_724delinsAAG ENSP00000482293.1:p.Lys241=
ENST00000620057.4:c.*927_*929delinsAAG ENSP00000481988.1:n.*927_*929delinsAAG
NM_000465.3:c.2261_2263delinsAAG NP_000456.2:p.Lys754=
NM_001282543.1:c.2204_2206delinsAAG NP_001269472.1:p.Lys735=
NM_001282545.1:c.908_910delinsAAG NP_001269474.1:p.Lys303=
NM_001282548.1:c.851_853delinsAAG NP_001269477.1:p.Lys284=
NM_001282549.1:c.722_724delinsAAG NP_001269478.1:p.Lys241=
NR_104212.1:n.2254_2256delinsAAG
NR_104215.1:n.2197_2199delinsAAG
NR_104216.1:n.1453_1455delinsAAG
XM_011511567.1:c.2207_2209delinsAAG XP_011509869.1:p.Lys736=
XM_017004613.1:c.2360_2362delinsAAG XP_016860102.1:p.Lys787=
XR_002959322.1:n.2627_2629delinsAAG
NM_000465.4:c.2261_2263delinsAAG MANE Select NP_000456.2:p.Lys754=
NM_001282543.2:c.2204_2206delinsAAG NP_001269472.1:p.Lys735=
NM_001282545.2:c.908_910delinsAAG NP_001269474.1:p.Lys303=
NM_001282548.2:c.851_853delinsAAG NP_001269477.1:p.Lys284=
NM_001282549.2:c.722_724delinsAAG NP_001269478.1:p.Lys241=
NR_104212.2:n.2226_2228delinsAAG
NR_104215.2:n.2169_2171delinsAAG
NR_104216.2:n.1425_1427delinsAAG