Canonical Allele Identifier: CA2091561645
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51942526C= , CM000675.2:g.51942526C= GRCh38
NC_000013.10:g.52516662C= , CM000675.1:g.52516662C= GRCh37
NC_000013.9:g.51414663C= NCBI36
NG_008806.1:g.73969G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*922G= ENSP00000489512.2:n.*922G=
ENST00000673864.2:c.*2016G= ENSP00000501045.2:n.*2016G=
ENST00000674147.2:c.2651G= ENSP00000500964.2:p.Cys884=
ENST00000242839.10:c.3272G= MANE Select ENSP00000242839.5:p.Cys1091=
ENST00000344297.9:c.2651G= ENSP00000342559.5:p.Cys884=
ENST00000400366.6:c.2939G= ENSP00000383217.3:p.Cys980=
ENST00000448424.7:c.3020G= ENSP00000416738.3:p.Cys1007=
ENST00000673772.1:c.3038G= ENSP00000501168.1:p.Cys1013=
ENST00000673867.1:n.3411G=
ENST00000674126.1:n.3635G=
ENST00000674147.1:c.2207G= ENSP00000500964.1:p.Cys736=
ENST00000242839.8:c.3272G= ENSP00000242839.4:p.Cys1091=
ENST00000344297.8:c.2651G= ENSP00000342559.5:p.Cys884=
ENST00000400366.5:c.2939G= ENSP00000383217.3:p.Cys980=
ENST00000400370.8:c.1982G= ENSP00000383221.3:p.Cys661=
ENST00000418097.7:c.3077G= ENSP00000393343.2:p.Cys1026=
ENST00000448424.6:c.3038G= ENSP00000416738.2:p.Cys1013=
ENST00000634296.1:c.1050G=
ENST00000634308.1:c.*373G= ENSP00000489234.1:n.*373G=
ENST00000634620.1:n.4016G=
ENST00000634810.1:n.2617G=
ENST00000634844.1:c.3128G= ENSP00000489398.1:p.Cys1043=
NM_000053.3:c.3272G= NP_000044.2:p.Cys1091=
NM_001005918.2:c.2651G= NP_001005918.1:p.Cys884=
NM_001243182.1:c.2939G= NP_001230111.1:p.Cys980=
XM_005266423.2:c.3176G= XP_005266480.1:p.Cys1059=
XM_005266424.3:c.3176G= XP_005266481.1:p.Cys1059=
XM_005266427.2:c.3038G= XP_005266484.1:p.Cys1013=
XM_005266428.1:c.3020G= XP_005266485.1:p.Cys1007=
XM_005266430.3:c.3272G= XP_005266487.1:p.Cys1091=
XM_005266431.2:c.3236G= XP_005266488.1:p.Cys1079=
XM_005266432.2:c.2786G= XP_005266489.1:p.Cys929=
XM_006719837.2:c.3176G= XP_006719900.1:p.Cys1059=
XM_006719838.1:c.1088G= XP_006719901.1:p.Cys363=
XM_006719839.1:c.905G= XP_006719902.1:p.Cys302=
XM_011535117.1:c.3176G= XP_011533419.1:p.Cys1059=
XM_011535118.1:c.3137G= XP_011533420.1:p.Cys1046=
XM_011535119.1:c.3089G= XP_011533421.1:p.Cys1030=
XM_011535120.1:c.2858G= XP_011533422.1:p.Cys953=
XM_011535121.1:c.2759G= XP_011533423.1:p.Cys920=
XM_011535122.1:c.1940G= XP_011533424.1:p.Cys647=
XR_941601.1:n.3491G=
XR_941602.1:n.3491G=
XR_941603.1:n.3491G=
XR_941604.1:n.3491G=
NM_001330578.1:c.3038G= NP_001317507.1:p.Cys1013=
NM_001330579.1:c.3020G= NP_001317508.1:p.Cys1007=
XM_005266424.4:c.3176G= XP_005266481.1:p.Cys1059=
XM_005266430.4:c.3272G= XP_005266487.1:p.Cys1091=
XM_005266431.4:c.3236G= XP_005266488.1:p.Cys1079=
XM_006719837.3:c.3176G= XP_006719900.1:p.Cys1059=
XM_011535117.3:c.3176G= XP_011533419.1:p.Cys1059=
XM_017020627.1:c.3176G= XP_016876116.1:p.Cys1059=
NM_000053.4:c.3272G= MANE Select NP_000044.2:p.Cys1091=
NM_001005918.3:c.2651G= NP_001005918.1:p.Cys884=
NM_001330579.2:c.3020G= NP_001317508.1:p.Cys1007=
NM_001243182.2:c.2939G= NP_001230111.1:p.Cys980=
NM_001330578.2:c.3038G= NP_001317507.1:p.Cys1013=