Canonical Allele Identifier: CA2091559499
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51941166G= , CM000675.2:g.51941166G= GRCh38
NC_000013.10:g.52515302G= , CM000675.1:g.52515302G= GRCh37
NC_000013.9:g.51413303G= NCBI36
NG_008806.1:g.75329C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1121C= ENSP00000489512.2:n.*1121C=
ENST00000673864.2:c.*2215C= ENSP00000501045.2:n.*2215C=
ENST00000674147.2:c.2850C= ENSP00000500964.2:p.Asn950=
ENST00000242839.10:c.3471C= MANE Select ENSP00000242839.5:p.Asn1157=
ENST00000344297.9:c.2850C= ENSP00000342559.5:p.Asn950=
ENST00000400366.6:c.3138C= ENSP00000383217.3:p.Asn1046=
ENST00000448424.7:c.3219C= ENSP00000416738.3:p.Asn1073=
ENST00000673772.1:c.3237C= ENSP00000501168.1:p.Asn1079=
ENST00000673867.1:n.3610C=
ENST00000674126.1:n.3834C=
ENST00000674147.1:c.2406C= ENSP00000500964.1:p.Asn802=
ENST00000242839.8:c.3471C= ENSP00000242839.4:p.Asn1157=
ENST00000344297.8:c.2850C= ENSP00000342559.5:p.Asn950=
ENST00000400366.5:c.3138C= ENSP00000383217.3:p.Asn1046=
ENST00000400370.8:c.2181C= ENSP00000383221.3:p.Asn727=
ENST00000418097.7:c.3276C= ENSP00000393343.2:p.Asn1092=
ENST00000448424.6:c.3237C= ENSP00000416738.2:p.Asn1079=
ENST00000634296.1:c.1249C=
ENST00000634308.1:c.*572C= ENSP00000489234.1:n.*572C=
ENST00000634620.1:n.4215C=
ENST00000634810.1:n.2816C=
ENST00000634844.1:c.3327C= ENSP00000489398.1:p.Asn1109=
NM_000053.3:c.3471C= NP_000044.2:p.Asn1157=
NM_001005918.2:c.2850C= NP_001005918.1:p.Asn950=
NM_001243182.1:c.3138C= NP_001230111.1:p.Asn1046=
XM_005266423.2:c.3375C= XP_005266480.1:p.Asn1125=
XM_005266424.3:c.3375C= XP_005266481.1:p.Asn1125=
XM_005266427.2:c.3237C= XP_005266484.1:p.Asn1079=
XM_005266428.1:c.3219C= XP_005266485.1:p.Asn1073=
XM_005266430.3:c.3471C= XP_005266487.1:p.Asn1157=
XM_005266431.2:c.3435C= XP_005266488.1:p.Asn1145=
XM_005266432.2:c.2985C= XP_005266489.1:p.Asn995=
XM_006719837.2:c.3375C= XP_006719900.1:p.Asn1125=
XM_006719838.1:c.1287C= XP_006719901.1:p.Asn429=
XM_006719839.1:c.1104C= XP_006719902.1:p.Asn368=
XM_011535117.1:c.3375C= XP_011533419.1:p.Asn1125=
XM_011535118.1:c.3336C= XP_011533420.1:p.Asn1112=
XM_011535119.1:c.3288C= XP_011533421.1:p.Asn1096=
XM_011535120.1:c.3057C= XP_011533422.1:p.Asn1019=
XM_011535121.1:c.2958C= XP_011533423.1:p.Asn986=
XM_011535122.1:c.2139C= XP_011533424.1:p.Asn713=
XR_941601.1:n.3690C=
XR_941602.1:n.3690C=
XR_941603.1:n.3690C=
XR_941604.1:n.3690C=
NM_001330578.1:c.3237C= NP_001317507.1:p.Asn1079=
NM_001330579.1:c.3219C= NP_001317508.1:p.Asn1073=
XM_005266424.4:c.3375C= XP_005266481.1:p.Asn1125=
XM_005266430.4:c.3471C= XP_005266487.1:p.Asn1157=
XM_005266431.4:c.3435C= XP_005266488.1:p.Asn1145=
XM_006719837.3:c.3375C= XP_006719900.1:p.Asn1125=
XM_011535117.3:c.3375C= XP_011533419.1:p.Asn1125=
XM_017020627.1:c.3375C= XP_016876116.1:p.Asn1125=
NM_000053.4:c.3471C= MANE Select NP_000044.2:p.Asn1157=
NM_001005918.3:c.2850C= NP_001005918.1:p.Asn950=
NM_001330579.2:c.3219C= NP_001317508.1:p.Asn1073=
NM_001243182.2:c.3138C= NP_001230111.1:p.Asn1046=
NM_001330578.2:c.3237C= NP_001317507.1:p.Asn1079=