Canonical Allele Identifier: CA2091563675
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51944113T= , CM000675.2:g.51944113T= GRCh38
NC_000013.10:g.52518249T= , CM000675.1:g.52518249T= GRCh37
NC_000013.9:g.51416250T= NCBI36
NG_008806.1:g.72382A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*894-1559A= ENSP00000489512.2:n.*894-1559A=
ENST00000673864.2:c.*1983A= ENSP00000501045.2:n.*1983A=
ENST00000674147.2:c.2618A= ENSP00000500964.2:p.Lys873=
ENST00000242839.10:c.3239A= MANE Select ENSP00000242839.5:p.Lys1080=
ENST00000344297.9:c.2618A= ENSP00000342559.5:p.Lys873=
ENST00000400366.6:c.2906A= ENSP00000383217.3:p.Lys969=
ENST00000448424.7:c.2987A= ENSP00000416738.3:p.Lys996=
ENST00000673772.1:c.3005A= ENSP00000501168.1:p.Lys1002=
ENST00000673867.1:n.3378A=
ENST00000674126.1:n.3602A=
ENST00000674147.1:c.2174A= ENSP00000500964.1:p.Lys725=
ENST00000242839.8:c.3239A= ENSP00000242839.4:p.Lys1080=
ENST00000344297.8:c.2618A= ENSP00000342559.5:p.Lys873=
ENST00000400366.5:c.2906A= ENSP00000383217.3:p.Lys969=
ENST00000400370.8:c.1949A= ENSP00000383221.3:p.Lys650=
ENST00000418097.7:c.3044A= ENSP00000393343.2:p.Lys1015=
ENST00000448424.6:c.3005A= ENSP00000416738.2:p.Lys1002=
ENST00000466629.1:n.459A=
ENST00000634296.1:c.1022-1559A=
ENST00000634308.1:c.*340A= ENSP00000489234.1:n.*340A=
ENST00000634620.1:n.3983A=
ENST00000634810.1:n.2584A=
ENST00000634844.1:c.3095A= ENSP00000489398.1:p.Lys1032=
NM_000053.3:c.3239A= NP_000044.2:p.Lys1080=
NM_001005918.2:c.2618A= NP_001005918.1:p.Lys873=
NM_001243182.1:c.2906A= NP_001230111.1:p.Lys969=
XM_005266423.2:c.3143A= XP_005266480.1:p.Lys1048=
XM_005266424.3:c.3143A= XP_005266481.1:p.Lys1048=
XM_005266427.2:c.3005A= XP_005266484.1:p.Lys1002=
XM_005266428.1:c.2987A= XP_005266485.1:p.Lys996=
XM_005266430.3:c.3239A= XP_005266487.1:p.Lys1080=
XM_005266431.2:c.3203A= XP_005266488.1:p.Lys1068=
XM_005266432.2:c.2753A= XP_005266489.1:p.Lys918=
XM_006719837.2:c.3143A= XP_006719900.1:p.Lys1048=
XM_006719838.1:c.1055A= XP_006719901.1:p.Lys352=
XM_006719839.1:c.877-1559A= XP_006719902.1:n.877-1559A=
XM_011535117.1:c.3143A= XP_011533419.1:p.Lys1048=
XM_011535118.1:c.3104A= XP_011533420.1:p.Lys1035=
XM_011535119.1:c.3061-1559A= XP_011533421.1:n.3061-1559A=
XM_011535120.1:c.2825A= XP_011533422.1:p.Lys942=
XM_011535121.1:c.2731-1559A= XP_011533423.1:n.2731-1559A=
XM_011535122.1:c.1907A= XP_011533424.1:p.Lys636=
XR_941601.1:n.3458A=
XR_941602.1:n.3458A=
XR_941603.1:n.3458A=
XR_941604.1:n.3458A=
NM_001330578.1:c.3005A= NP_001317507.1:p.Lys1002=
NM_001330579.1:c.2987A= NP_001317508.1:p.Lys996=
XM_005266424.4:c.3143A= XP_005266481.1:p.Lys1048=
XM_005266430.4:c.3239A= XP_005266487.1:p.Lys1080=
XM_005266431.4:c.3203A= XP_005266488.1:p.Lys1068=
XM_006719837.3:c.3143A= XP_006719900.1:p.Lys1048=
XM_011535117.3:c.3143A= XP_011533419.1:p.Lys1048=
XM_017020627.1:c.3143A= XP_016876116.1:p.Lys1048=
NM_000053.4:c.3239A= MANE Select NP_000044.2:p.Lys1080=
NM_001005918.3:c.2618A= NP_001005918.1:p.Lys873=
NM_001330579.2:c.2987A= NP_001317508.1:p.Lys996=
NM_001243182.2:c.2906A= NP_001230111.1:p.Lys969=
NM_001330578.2:c.3005A= NP_001317507.1:p.Lys1002=