Canonical Allele Identifier: CA2091559398
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51941120C= , CM000675.2:g.51941120C= GRCh38
NC_000013.10:g.52515256C= , CM000675.1:g.52515256C= GRCh37
NC_000013.9:g.51413257C= NCBI36
NG_008806.1:g.75375G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1167G= ENSP00000489512.2:n.*1167G=
ENST00000673864.2:c.*2261G= ENSP00000501045.2:n.*2261G=
ENST00000674147.2:c.2896G= ENSP00000500964.2:p.Glu966=
ENST00000242839.10:c.3517G= MANE Select ENSP00000242839.5:p.Glu1173=
ENST00000344297.9:c.2896G= ENSP00000342559.5:p.Glu966=
ENST00000400366.6:c.3184G= ENSP00000383217.3:p.Glu1062=
ENST00000448424.7:c.3265G= ENSP00000416738.3:p.Glu1089=
ENST00000673772.1:c.3283G= ENSP00000501168.1:p.Glu1095=
ENST00000673867.1:n.3656G=
ENST00000674126.1:n.3880G=
ENST00000674147.1:c.2452G= ENSP00000500964.1:p.Glu818=
ENST00000242839.8:c.3517G= ENSP00000242839.4:p.Glu1173=
ENST00000344297.8:c.2896G= ENSP00000342559.5:p.Glu966=
ENST00000400366.5:c.3184G= ENSP00000383217.3:p.Glu1062=
ENST00000400370.8:c.2227G= ENSP00000383221.3:p.Glu743=
ENST00000418097.7:c.3322G= ENSP00000393343.2:p.Glu1108=
ENST00000448424.6:c.3283G= ENSP00000416738.2:p.Glu1095=
ENST00000634296.1:c.1295G=
ENST00000634308.1:c.*618G= ENSP00000489234.1:n.*618G=
ENST00000634620.1:n.4261G=
ENST00000634810.1:n.2862G=
ENST00000634844.1:c.3373G= ENSP00000489398.1:p.Glu1125=
NM_000053.3:c.3517G= NP_000044.2:p.Glu1173=
NM_001005918.2:c.2896G= NP_001005918.1:p.Glu966=
NM_001243182.1:c.3184G= NP_001230111.1:p.Glu1062=
XM_005266423.2:c.3421G= XP_005266480.1:p.Glu1141=
XM_005266424.3:c.3421G= XP_005266481.1:p.Glu1141=
XM_005266427.2:c.3283G= XP_005266484.1:p.Glu1095=
XM_005266428.1:c.3265G= XP_005266485.1:p.Glu1089=
XM_005266430.3:c.3517G= XP_005266487.1:p.Glu1173=
XM_005266431.2:c.3481G= XP_005266488.1:p.Glu1161=
XM_005266432.2:c.3031G= XP_005266489.1:p.Glu1011=
XM_006719837.2:c.3421G= XP_006719900.1:p.Glu1141=
XM_006719838.1:c.1333G= XP_006719901.1:p.Glu445=
XM_006719839.1:c.1150G= XP_006719902.1:p.Glu384=
XM_011535117.1:c.3421G= XP_011533419.1:p.Glu1141=
XM_011535118.1:c.3382G= XP_011533420.1:p.Glu1128=
XM_011535119.1:c.3334G= XP_011533421.1:p.Glu1112=
XM_011535120.1:c.3103G= XP_011533422.1:p.Glu1035=
XM_011535121.1:c.3004G= XP_011533423.1:p.Glu1002=
XM_011535122.1:c.2185G= XP_011533424.1:p.Glu729=
XR_941601.1:n.3736G=
XR_941602.1:n.3736G=
XR_941603.1:n.3736G=
XR_941604.1:n.3736G=
NM_001330578.1:c.3283G= NP_001317507.1:p.Glu1095=
NM_001330579.1:c.3265G= NP_001317508.1:p.Glu1089=
XM_005266424.4:c.3421G= XP_005266481.1:p.Glu1141=
XM_005266430.4:c.3517G= XP_005266487.1:p.Glu1173=
XM_005266431.4:c.3481G= XP_005266488.1:p.Glu1161=
XM_006719837.3:c.3421G= XP_006719900.1:p.Glu1141=
XM_011535117.3:c.3421G= XP_011533419.1:p.Glu1141=
XM_017020627.1:c.3421G= XP_016876116.1:p.Glu1141=
NM_000053.4:c.3517G= MANE Select NP_000044.2:p.Glu1173=
NM_001005918.3:c.2896G= NP_001005918.1:p.Glu966=
NM_001330579.2:c.3265G= NP_001317508.1:p.Glu1089=
NM_001243182.2:c.3184G= NP_001230111.1:p.Glu1062=
NM_001330578.2:c.3283G= NP_001317507.1:p.Glu1095=