Canonical Allele Identifier: CA2091559606
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51941212T= , CM000675.2:g.51941212T= GRCh38
NC_000013.10:g.52515348T= , CM000675.1:g.52515348T= GRCh37
NC_000013.9:g.51413349T= NCBI36
NG_008806.1:g.75283A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1075A= ENSP00000489512.2:n.*1075A=
ENST00000673864.2:c.*2169A= ENSP00000501045.2:n.*2169A=
ENST00000674147.2:c.2804A= ENSP00000500964.2:p.Gln935=
ENST00000242839.10:c.3425A= MANE Select ENSP00000242839.5:p.Gln1142=
ENST00000344297.9:c.2804A= ENSP00000342559.5:p.Gln935=
ENST00000400366.6:c.3092A= ENSP00000383217.3:p.Gln1031=
ENST00000448424.7:c.3173A= ENSP00000416738.3:p.Gln1058=
ENST00000673772.1:c.3191A= ENSP00000501168.1:p.Gln1064=
ENST00000673867.1:n.3564A=
ENST00000674126.1:n.3788A=
ENST00000674147.1:c.2360A= ENSP00000500964.1:p.Gln787=
ENST00000242839.8:c.3425A= ENSP00000242839.4:p.Gln1142=
ENST00000344297.8:c.2804A= ENSP00000342559.5:p.Gln935=
ENST00000400366.5:c.3092A= ENSP00000383217.3:p.Gln1031=
ENST00000400370.8:c.2135A= ENSP00000383221.3:p.Gln712=
ENST00000418097.7:c.3230A= ENSP00000393343.2:p.Gln1077=
ENST00000448424.6:c.3191A= ENSP00000416738.2:p.Gln1064=
ENST00000634296.1:c.1203A=
ENST00000634308.1:c.*526A= ENSP00000489234.1:n.*526A=
ENST00000634620.1:n.4169A=
ENST00000634810.1:n.2770A=
ENST00000634844.1:c.3281A= ENSP00000489398.1:p.Gln1094=
NM_000053.3:c.3425A= NP_000044.2:p.Gln1142=
NM_001005918.2:c.2804A= NP_001005918.1:p.Gln935=
NM_001243182.1:c.3092A= NP_001230111.1:p.Gln1031=
XM_005266423.2:c.3329A= XP_005266480.1:p.Gln1110=
XM_005266424.3:c.3329A= XP_005266481.1:p.Gln1110=
XM_005266427.2:c.3191A= XP_005266484.1:p.Gln1064=
XM_005266428.1:c.3173A= XP_005266485.1:p.Gln1058=
XM_005266430.3:c.3425A= XP_005266487.1:p.Gln1142=
XM_005266431.2:c.3389A= XP_005266488.1:p.Gln1130=
XM_005266432.2:c.2939A= XP_005266489.1:p.Gln980=
XM_006719837.2:c.3329A= XP_006719900.1:p.Gln1110=
XM_006719838.1:c.1241A= XP_006719901.1:p.Gln414=
XM_006719839.1:c.1058A= XP_006719902.1:p.Gln353=
XM_011535117.1:c.3329A= XP_011533419.1:p.Gln1110=
XM_011535118.1:c.3290A= XP_011533420.1:p.Gln1097=
XM_011535119.1:c.3242A= XP_011533421.1:p.Gln1081=
XM_011535120.1:c.3011A= XP_011533422.1:p.Gln1004=
XM_011535121.1:c.2912A= XP_011533423.1:p.Gln971=
XM_011535122.1:c.2093A= XP_011533424.1:p.Gln698=
XR_941601.1:n.3644A=
XR_941602.1:n.3644A=
XR_941603.1:n.3644A=
XR_941604.1:n.3644A=
NM_001330578.1:c.3191A= NP_001317507.1:p.Gln1064=
NM_001330579.1:c.3173A= NP_001317508.1:p.Gln1058=
XM_005266424.4:c.3329A= XP_005266481.1:p.Gln1110=
XM_005266430.4:c.3425A= XP_005266487.1:p.Gln1142=
XM_005266431.4:c.3389A= XP_005266488.1:p.Gln1130=
XM_006719837.3:c.3329A= XP_006719900.1:p.Gln1110=
XM_011535117.3:c.3329A= XP_011533419.1:p.Gln1110=
XM_017020627.1:c.3329A= XP_016876116.1:p.Gln1110=
NM_000053.4:c.3425A= MANE Select NP_000044.2:p.Gln1142=
NM_001005918.3:c.2804A= NP_001005918.1:p.Gln935=
NM_001330579.2:c.3173A= NP_001317508.1:p.Gln1058=
NM_001243182.2:c.3092A= NP_001230111.1:p.Gln1031=
NM_001330578.2:c.3191A= NP_001317507.1:p.Gln1064=