Canonical Allele Identifier: CA2091559612
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51941215G= , CM000675.2:g.51941215G= GRCh38
NC_000013.10:g.52515351G= , CM000675.1:g.52515351G= GRCh37
NC_000013.9:g.51413352G= NCBI36
NG_008806.1:g.75280C=

Transcript Alleles

HGVS Amino-acid change
ENST00000634296.2:c.*1072C= ENSP00000489512.2:n.*1072C=
ENST00000673864.2:c.*2166C= ENSP00000501045.2:n.*2166C=
ENST00000674147.2:c.2801C= ENSP00000500964.2:p.Pro934=
ENST00000242839.10:c.3422C= MANE Select ENSP00000242839.5:p.Pro1141=
ENST00000344297.9:c.2801C= ENSP00000342559.5:p.Pro934=
ENST00000400366.6:c.3089C= ENSP00000383217.3:p.Pro1030=
ENST00000448424.7:c.3170C= ENSP00000416738.3:p.Pro1057=
ENST00000673772.1:c.3188C= ENSP00000501168.1:p.Pro1063=
ENST00000673867.1:n.3561C=
ENST00000674126.1:n.3785C=
ENST00000674147.1:c.2357C= ENSP00000500964.1:p.Pro786=
ENST00000242839.8:c.3422C= ENSP00000242839.4:p.Pro1141=
ENST00000344297.8:c.2801C= ENSP00000342559.5:p.Pro934=
ENST00000400366.5:c.3089C= ENSP00000383217.3:p.Pro1030=
ENST00000400370.8:c.2132C= ENSP00000383221.3:p.Pro711=
ENST00000418097.7:c.3227C= ENSP00000393343.2:p.Pro1076=
ENST00000448424.6:c.3188C= ENSP00000416738.2:p.Pro1063=
ENST00000634296.1:c.1200C=
ENST00000634308.1:c.*523C= ENSP00000489234.1:n.*523C=
ENST00000634620.1:n.4166C=
ENST00000634810.1:n.2767C=
ENST00000634844.1:c.3278C= ENSP00000489398.1:p.Pro1093=
NM_000053.3:c.3422C= NP_000044.2:p.Pro1141=
NM_001005918.2:c.2801C= NP_001005918.1:p.Pro934=
NM_001243182.1:c.3089C= NP_001230111.1:p.Pro1030=
XM_005266423.2:c.3326C= XP_005266480.1:p.Pro1109=
XM_005266424.3:c.3326C= XP_005266481.1:p.Pro1109=
XM_005266427.2:c.3188C= XP_005266484.1:p.Pro1063=
XM_005266428.1:c.3170C= XP_005266485.1:p.Pro1057=
XM_005266430.3:c.3422C= XP_005266487.1:p.Pro1141=
XM_005266431.2:c.3386C= XP_005266488.1:p.Pro1129=
XM_005266432.2:c.2936C= XP_005266489.1:p.Pro979=
XM_006719837.2:c.3326C= XP_006719900.1:p.Pro1109=
XM_006719838.1:c.1238C= XP_006719901.1:p.Pro413=
XM_006719839.1:c.1055C= XP_006719902.1:p.Pro352=
XM_011535117.1:c.3326C= XP_011533419.1:p.Pro1109=
XM_011535118.1:c.3287C= XP_011533420.1:p.Pro1096=
XM_011535119.1:c.3239C= XP_011533421.1:p.Pro1080=
XM_011535120.1:c.3008C= XP_011533422.1:p.Pro1003=
XM_011535121.1:c.2909C= XP_011533423.1:p.Pro970=
XM_011535122.1:c.2090C= XP_011533424.1:p.Pro697=
XR_941601.1:n.3641C=
XR_941602.1:n.3641C=
XR_941603.1:n.3641C=
XR_941604.1:n.3641C=
NM_001330578.1:c.3188C= NP_001317507.1:p.Pro1063=
NM_001330579.1:c.3170C= NP_001317508.1:p.Pro1057=
XM_005266424.4:c.3326C= XP_005266481.1:p.Pro1109=
XM_005266430.4:c.3422C= XP_005266487.1:p.Pro1141=
XM_005266431.4:c.3386C= XP_005266488.1:p.Pro1129=
XM_006719837.3:c.3326C= XP_006719900.1:p.Pro1109=
XM_011535117.3:c.3326C= XP_011533419.1:p.Pro1109=
XM_017020627.1:c.3326C= XP_016876116.1:p.Pro1109=
NM_000053.4:c.3422C= MANE Select NP_000044.2:p.Pro1141=
NM_001005918.3:c.2801C= NP_001005918.1:p.Pro934=
NM_001330579.2:c.3170C= NP_001317508.1:p.Pro1057=
NM_001243182.2:c.3089C= NP_001230111.1:p.Pro1030=
NM_001330578.2:c.3188C= NP_001317507.1:p.Pro1063=