Canonical Allele Identifier: CA2091561668
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51942537G= , CM000675.2:g.51942537G= GRCh38
NC_000013.10:g.52516673G= , CM000675.1:g.52516673G= GRCh37
NC_000013.9:g.51414674G= NCBI36
NG_008806.1:g.73958C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*911C= ENSP00000489512.2:n.*911C=
ENST00000673864.2:c.*2005C= ENSP00000501045.2:n.*2005C=
ENST00000674147.2:c.2640C= ENSP00000500964.2:p.Thr880=
ENST00000242839.10:c.3261C= MANE Select ENSP00000242839.5:p.Thr1087=
ENST00000344297.9:c.2640C= ENSP00000342559.5:p.Thr880=
ENST00000400366.6:c.2928C= ENSP00000383217.3:p.Thr976=
ENST00000448424.7:c.3009C= ENSP00000416738.3:p.Thr1003=
ENST00000673772.1:c.3027C= ENSP00000501168.1:p.Thr1009=
ENST00000673867.1:n.3400C=
ENST00000674126.1:n.3624C=
ENST00000674147.1:c.2196C= ENSP00000500964.1:p.Thr732=
ENST00000242839.8:c.3261C= ENSP00000242839.4:p.Thr1087=
ENST00000344297.8:c.2640C= ENSP00000342559.5:p.Thr880=
ENST00000400366.5:c.2928C= ENSP00000383217.3:p.Thr976=
ENST00000400370.8:c.1971C= ENSP00000383221.3:p.Thr657=
ENST00000418097.7:c.3066C= ENSP00000393343.2:p.Thr1022=
ENST00000448424.6:c.3027C= ENSP00000416738.2:p.Thr1009=
ENST00000634296.1:c.1039C=
ENST00000634308.1:c.*362C= ENSP00000489234.1:n.*362C=
ENST00000634620.1:n.4005C=
ENST00000634810.1:n.2606C=
ENST00000634844.1:c.3117C= ENSP00000489398.1:p.Thr1039=
NM_000053.3:c.3261C= NP_000044.2:p.Thr1087=
NM_001005918.2:c.2640C= NP_001005918.1:p.Thr880=
NM_001243182.1:c.2928C= NP_001230111.1:p.Thr976=
XM_005266423.2:c.3165C= XP_005266480.1:p.Thr1055=
XM_005266424.3:c.3165C= XP_005266481.1:p.Thr1055=
XM_005266427.2:c.3027C= XP_005266484.1:p.Thr1009=
XM_005266428.1:c.3009C= XP_005266485.1:p.Thr1003=
XM_005266430.3:c.3261C= XP_005266487.1:p.Thr1087=
XM_005266431.2:c.3225C= XP_005266488.1:p.Thr1075=
XM_005266432.2:c.2775C= XP_005266489.1:p.Thr925=
XM_006719837.2:c.3165C= XP_006719900.1:p.Thr1055=
XM_006719838.1:c.1077C= XP_006719901.1:p.Thr359=
XM_006719839.1:c.894C= XP_006719902.1:p.Thr298=
XM_011535117.1:c.3165C= XP_011533419.1:p.Thr1055=
XM_011535118.1:c.3126C= XP_011533420.1:p.Thr1042=
XM_011535119.1:c.3078C= XP_011533421.1:p.Thr1026=
XM_011535120.1:c.2847C= XP_011533422.1:p.Thr949=
XM_011535121.1:c.2748C= XP_011533423.1:p.Thr916=
XM_011535122.1:c.1929C= XP_011533424.1:p.Thr643=
XR_941601.1:n.3480C=
XR_941602.1:n.3480C=
XR_941603.1:n.3480C=
XR_941604.1:n.3480C=
NM_001330578.1:c.3027C= NP_001317507.1:p.Thr1009=
NM_001330579.1:c.3009C= NP_001317508.1:p.Thr1003=
XM_005266424.4:c.3165C= XP_005266481.1:p.Thr1055=
XM_005266430.4:c.3261C= XP_005266487.1:p.Thr1087=
XM_005266431.4:c.3225C= XP_005266488.1:p.Thr1075=
XM_006719837.3:c.3165C= XP_006719900.1:p.Thr1055=
XM_011535117.3:c.3165C= XP_011533419.1:p.Thr1055=
XM_017020627.1:c.3165C= XP_016876116.1:p.Thr1055=
NM_000053.4:c.3261C= MANE Select NP_000044.2:p.Thr1087=
NM_001005918.3:c.2640C= NP_001005918.1:p.Thr880=
NM_001330579.2:c.3009C= NP_001317508.1:p.Thr1003=
NM_001243182.2:c.2928C= NP_001230111.1:p.Thr976=
NM_001330578.2:c.3027C= NP_001317507.1:p.Thr1009=