Canonical Allele Identifier: CA2091556935
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51939172G= , CM000675.2:g.51939172G= GRCh38
NC_000013.10:g.52513308G= , CM000675.1:g.52513308G= GRCh37
NC_000013.9:g.51411309G= NCBI36
NG_008806.1:g.77323C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1228C= ENSP00000489512.2:n.*1228C=
ENST00000673864.2:c.*2322C= ENSP00000501045.2:n.*2322C=
ENST00000674147.2:c.2957C= ENSP00000500964.2:p.Ala986=
ENST00000242839.10:c.3578C= MANE Select ENSP00000242839.5:p.Ala1193=
ENST00000344297.9:c.2957C= ENSP00000342559.5:p.Ala986=
ENST00000400366.6:c.3245C= ENSP00000383217.3:p.Ala1082=
ENST00000448424.7:c.3326C= ENSP00000416738.3:p.Ala1109=
ENST00000673696.1:n.819C=
ENST00000673772.1:c.3344C= ENSP00000501168.1:p.Ala1115=
ENST00000673867.1:n.3717C=
ENST00000673923.1:n.444C=
ENST00000674147.1:c.2513C= ENSP00000500964.1:p.Ala838=
ENST00000242839.8:c.3578C= ENSP00000242839.4:p.Ala1193=
ENST00000344297.8:c.2957C= ENSP00000342559.5:p.Ala986=
ENST00000400366.5:c.3245C= ENSP00000383217.3:p.Ala1082=
ENST00000400370.8:c.2288C= ENSP00000383221.3:p.Ala763=
ENST00000418097.7:c.3383C= ENSP00000393343.2:p.Ala1128=
ENST00000448424.6:c.3344C= ENSP00000416738.2:p.Ala1115=
ENST00000634296.1:c.1356C=
ENST00000634308.1:c.*679C= ENSP00000489234.1:n.*679C=
ENST00000634620.1:n.4322C=
ENST00000634810.1:n.2923C=
ENST00000634844.1:c.3434C= ENSP00000489398.1:p.Ala1145=
NM_000053.3:c.3578C= NP_000044.2:p.Ala1193=
NM_001005918.2:c.2957C= NP_001005918.1:p.Ala986=
NM_001243182.1:c.3245C= NP_001230111.1:p.Ala1082=
XM_005266423.2:c.3482C= XP_005266480.1:p.Ala1161=
XM_005266424.3:c.3482C= XP_005266481.1:p.Ala1161=
XM_005266427.2:c.3344C= XP_005266484.1:p.Ala1115=
XM_005266428.1:c.3326C= XP_005266485.1:p.Ala1109=
XM_005266430.3:c.3578C= XP_005266487.1:p.Ala1193=
XM_005266431.2:c.3542C= XP_005266488.1:p.Ala1181=
XM_005266432.2:c.3092C= XP_005266489.1:p.Ala1031=
XM_006719837.2:c.3482C= XP_006719900.1:p.Ala1161=
XM_006719838.1:c.1394C= XP_006719901.1:p.Ala465=
XM_006719839.1:c.1211C= XP_006719902.1:p.Ala404=
XM_011535117.1:c.3482C= XP_011533419.1:p.Ala1161=
XM_011535118.1:c.3443C= XP_011533420.1:p.Ala1148=
XM_011535119.1:c.3395C= XP_011533421.1:p.Ala1132=
XM_011535120.1:c.3164C= XP_011533422.1:p.Ala1055=
XM_011535121.1:c.3065C= XP_011533423.1:p.Ala1022=
XM_011535122.1:c.2246C= XP_011533424.1:p.Ala749=
XR_941601.1:n.3797C=
XR_941602.1:n.3797C=
XR_941603.1:n.3797C=
XR_941604.1:n.3797C=
NM_001330578.1:c.3344C= NP_001317507.1:p.Ala1115=
NM_001330579.1:c.3326C= NP_001317508.1:p.Ala1109=
XM_005266424.4:c.3482C= XP_005266481.1:p.Ala1161=
XM_005266430.4:c.3578C= XP_005266487.1:p.Ala1193=
XM_005266431.4:c.3542C= XP_005266488.1:p.Ala1181=
XM_006719837.3:c.3482C= XP_006719900.1:p.Ala1161=
XM_011535117.3:c.3482C= XP_011533419.1:p.Ala1161=
XM_017020627.1:c.3482C= XP_016876116.1:p.Ala1161=
NM_000053.4:c.3578C= MANE Select NP_000044.2:p.Ala1193=
NM_001005918.3:c.2957C= NP_001005918.1:p.Ala986=
NM_001330579.2:c.3326C= NP_001317508.1:p.Ala1109=
NM_001243182.2:c.3245C= NP_001230111.1:p.Ala1082=
NM_001330578.2:c.3344C= NP_001317507.1:p.Ala1115=