Canonical Allele Identifier: CA2091556875
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51939145G= , CM000675.2:g.51939145G= GRCh38
NC_000013.10:g.52513281G= , CM000675.1:g.52513281G= GRCh37
NC_000013.9:g.51411282G= NCBI36
NG_008806.1:g.77350C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1255C= ENSP00000489512.2:n.*1255C=
ENST00000673864.2:c.*2349C= ENSP00000501045.2:n.*2349C=
ENST00000674147.2:c.2984C= ENSP00000500964.2:p.Ala995=
ENST00000242839.10:c.3605C= MANE Select ENSP00000242839.5:p.Ala1202=
ENST00000344297.9:c.2984C= ENSP00000342559.5:p.Ala995=
ENST00000400366.6:c.3272C= ENSP00000383217.3:p.Ala1091=
ENST00000448424.7:c.3353C= ENSP00000416738.3:p.Ala1118=
ENST00000673696.1:n.846C=
ENST00000673772.1:c.3371C= ENSP00000501168.1:p.Ala1124=
ENST00000673867.1:n.3744C=
ENST00000673923.1:n.471C=
ENST00000674147.1:c.2540C= ENSP00000500964.1:p.Ala847=
ENST00000242839.8:c.3605C= ENSP00000242839.4:p.Ala1202=
ENST00000344297.8:c.2984C= ENSP00000342559.5:p.Ala995=
ENST00000400366.5:c.3272C= ENSP00000383217.3:p.Ala1091=
ENST00000400370.8:c.2315C= ENSP00000383221.3:p.Ala772=
ENST00000418097.7:c.3410C= ENSP00000393343.2:p.Ala1137=
ENST00000448424.6:c.3371C= ENSP00000416738.2:p.Ala1124=
ENST00000634296.1:c.1383C=
ENST00000634308.1:c.*706C= ENSP00000489234.1:n.*706C=
ENST00000634620.1:n.4349C=
ENST00000634810.1:n.2950C=
ENST00000634844.1:c.3461C= ENSP00000489398.1:p.Ala1154=
NM_000053.3:c.3605C= NP_000044.2:p.Ala1202=
NM_001005918.2:c.2984C= NP_001005918.1:p.Ala995=
NM_001243182.1:c.3272C= NP_001230111.1:p.Ala1091=
XM_005266423.2:c.3509C= XP_005266480.1:p.Ala1170=
XM_005266424.3:c.3509C= XP_005266481.1:p.Ala1170=
XM_005266427.2:c.3371C= XP_005266484.1:p.Ala1124=
XM_005266428.1:c.3353C= XP_005266485.1:p.Ala1118=
XM_005266430.3:c.3605C= XP_005266487.1:p.Ala1202=
XM_005266431.2:c.3569C= XP_005266488.1:p.Ala1190=
XM_005266432.2:c.3119C= XP_005266489.1:p.Ala1040=
XM_006719837.2:c.3509C= XP_006719900.1:p.Ala1170=
XM_006719838.1:c.1421C= XP_006719901.1:p.Ala474=
XM_006719839.1:c.1238C= XP_006719902.1:p.Ala413=
XM_011535117.1:c.3509C= XP_011533419.1:p.Ala1170=
XM_011535118.1:c.3470C= XP_011533420.1:p.Ala1157=
XM_011535119.1:c.3422C= XP_011533421.1:p.Ala1141=
XM_011535120.1:c.3191C= XP_011533422.1:p.Ala1064=
XM_011535121.1:c.3092C= XP_011533423.1:p.Ala1031=
XM_011535122.1:c.2273C= XP_011533424.1:p.Ala758=
XR_941601.1:n.3824C=
XR_941602.1:n.3824C=
XR_941603.1:n.3824C=
XR_941604.1:n.3824C=
NM_001330578.1:c.3371C= NP_001317507.1:p.Ala1124=
NM_001330579.1:c.3353C= NP_001317508.1:p.Ala1118=
XM_005266424.4:c.3509C= XP_005266481.1:p.Ala1170=
XM_005266430.4:c.3605C= XP_005266487.1:p.Ala1202=
XM_005266431.4:c.3569C= XP_005266488.1:p.Ala1190=
XM_006719837.3:c.3509C= XP_006719900.1:p.Ala1170=
XM_011535117.3:c.3509C= XP_011533419.1:p.Ala1170=
XM_017020627.1:c.3509C= XP_016876116.1:p.Ala1170=
NM_000053.4:c.3605C= MANE Select NP_000044.2:p.Ala1202=
NM_001005918.3:c.2984C= NP_001005918.1:p.Ala995=
NM_001330579.2:c.3353C= NP_001317508.1:p.Ala1118=
NM_001243182.2:c.3272C= NP_001230111.1:p.Ala1091=
NM_001330578.2:c.3371C= NP_001317507.1:p.Ala1124=