Canonical Allele Identifier: CA2091566225
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51946471T= , CM000675.2:g.51946471T= GRCh38
NC_000013.10:g.52520607T= , CM000675.1:g.52520607T= GRCh37
NC_000013.9:g.51418608T= NCBI36
NG_008806.1:g.70024A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*706A= ENSP00000489512.2:n.*706A=
ENST00000673864.2:c.*1617A= ENSP00000501045.2:n.*1617A=
ENST00000674147.2:c.2252A= ENSP00000500964.2:p.Asn751=
ENST00000242839.10:c.2873A= MANE Select ENSP00000242839.5:p.Asn958=
ENST00000344297.9:c.2252A= ENSP00000342559.5:p.Asn751=
ENST00000400366.6:c.2540A= ENSP00000383217.3:p.Asn847=
ENST00000448424.7:c.2621A= ENSP00000416738.3:p.Asn874=
ENST00000673772.1:c.2639A= ENSP00000501168.1:p.Asn880=
ENST00000673867.1:n.1020A=
ENST00000674126.1:n.3236A=
ENST00000674147.1:c.1808A= ENSP00000500964.1:p.Asn603=
ENST00000242839.8:c.2873A= ENSP00000242839.4:p.Asn958=
ENST00000344297.8:c.2252A= ENSP00000342559.5:p.Asn751=
ENST00000400366.5:c.2540A= ENSP00000383217.3:p.Asn847=
ENST00000400370.8:c.1583A= ENSP00000383221.3:p.Asn528=
ENST00000418097.7:c.2866-2180A= ENSP00000393343.2:n.2866-2180A=
ENST00000448424.6:c.2639A= ENSP00000416738.2:p.Asn880=
ENST00000466629.1:n.93A=
ENST00000634296.1:c.834A=
ENST00000634308.1:c.2659A= ENSP00000489234.1:p.Thr887=
ENST00000634620.1:n.3617A=
ENST00000634810.1:n.2218A=
ENST00000634844.1:c.2729A= ENSP00000489398.1:p.Asn910=
ENST00000635406.1:n.219A=
NM_000053.3:c.2873A= NP_000044.2:p.Asn958=
NM_001005918.2:c.2252A= NP_001005918.1:p.Asn751=
NM_001243182.1:c.2540A= NP_001230111.1:p.Asn847=
XM_005266423.2:c.2777A= XP_005266480.1:p.Asn926=
XM_005266424.3:c.2777A= XP_005266481.1:p.Asn926=
XM_005266427.2:c.2639A= XP_005266484.1:p.Asn880=
XM_005266428.1:c.2621A= XP_005266485.1:p.Asn874=
XM_005266430.3:c.2873A= XP_005266487.1:p.Asn958=
XM_005266431.2:c.2837A= XP_005266488.1:p.Asn946=
XM_005266432.2:c.2387A= XP_005266489.1:p.Asn796=
XM_006719837.2:c.2777A= XP_006719900.1:p.Asn926=
XM_006719838.1:c.689A= XP_006719901.1:p.Asn230=
XM_006719839.1:c.689A= XP_006719902.1:p.Asn230=
XM_011535117.1:c.2777A= XP_011533419.1:p.Asn926=
XM_011535118.1:c.2738A= XP_011533420.1:p.Asn913=
XM_011535119.1:c.2873A= XP_011533421.1:p.Asn958=
XM_011535120.1:c.2459A= XP_011533422.1:p.Asn820=
XM_011535121.1:c.2730+3536A= XP_011533423.1:n.2730+3536A=
XM_011535122.1:c.1541A= XP_011533424.1:p.Asn514=
XR_941601.1:n.3092A=
XR_941602.1:n.3092A=
XR_941603.1:n.3092A=
XR_941604.1:n.3092A=
NM_001330578.1:c.2639A= NP_001317507.1:p.Asn880=
NM_001330579.1:c.2621A= NP_001317508.1:p.Asn874=
XM_005266424.4:c.2777A= XP_005266481.1:p.Asn926=
XM_005266430.4:c.2873A= XP_005266487.1:p.Asn958=
XM_005266431.4:c.2837A= XP_005266488.1:p.Asn946=
XM_006719837.3:c.2777A= XP_006719900.1:p.Asn926=
XM_011535117.3:c.2777A= XP_011533419.1:p.Asn926=
XM_017020627.1:c.2777A= XP_016876116.1:p.Asn926=
NM_000053.4:c.2873A= MANE Select NP_000044.2:p.Asn958=
NM_001005918.3:c.2252A= NP_001005918.1:p.Asn751=
NM_001330579.2:c.2621A= NP_001317508.1:p.Asn874=
NM_001243182.2:c.2540A= NP_001230111.1:p.Asn847=
NM_001330578.2:c.2639A= NP_001317507.1:p.Asn880=