Canonical Allele Identifier: CA2091566190
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51946404G= , CM000675.2:g.51946404G= GRCh38
NC_000013.10:g.52520540G= , CM000675.1:g.52520540G= GRCh37
NC_000013.9:g.51418541G= NCBI36
NG_008806.1:g.70091C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*773C= ENSP00000489512.2:n.*773C=
ENST00000673864.2:c.*1684C= ENSP00000501045.2:n.*1684C=
ENST00000674147.2:c.2319C= ENSP00000500964.2:p.Cys773=
ENST00000242839.10:c.2940C= MANE Select ENSP00000242839.5:p.Cys980=
ENST00000344297.9:c.2319C= ENSP00000342559.5:p.Cys773=
ENST00000400366.6:c.2607C= ENSP00000383217.3:p.Cys869=
ENST00000448424.7:c.2688C= ENSP00000416738.3:p.Cys896=
ENST00000673772.1:c.2706C= ENSP00000501168.1:p.Cys902=
ENST00000673867.1:n.1087C=
ENST00000674126.1:n.3303C=
ENST00000674147.1:c.1875C= ENSP00000500964.1:p.Cys625=
ENST00000242839.8:c.2940C= ENSP00000242839.4:p.Cys980=
ENST00000344297.8:c.2319C= ENSP00000342559.5:p.Cys773=
ENST00000400366.5:c.2607C= ENSP00000383217.3:p.Cys869=
ENST00000400370.8:c.1650C= ENSP00000383221.3:p.Cys550=
ENST00000418097.7:c.2866-2113C= ENSP00000393343.2:n.2866-2113C=
ENST00000448424.6:c.2706C= ENSP00000416738.2:p.Cys902=
ENST00000466629.1:n.160C=
ENST00000634296.1:c.901C=
ENST00000634308.1:c.*41C= ENSP00000489234.1:n.*41C=
ENST00000634620.1:n.3684C=
ENST00000634810.1:n.2285C=
ENST00000634844.1:c.2796C= ENSP00000489398.1:p.Cys932=
ENST00000635406.1:n.286C=
NM_000053.3:c.2940C= NP_000044.2:p.Cys980=
NM_001005918.2:c.2319C= NP_001005918.1:p.Cys773=
NM_001243182.1:c.2607C= NP_001230111.1:p.Cys869=
XM_005266423.2:c.2844C= XP_005266480.1:p.Cys948=
XM_005266424.3:c.2844C= XP_005266481.1:p.Cys948=
XM_005266427.2:c.2706C= XP_005266484.1:p.Cys902=
XM_005266428.1:c.2688C= XP_005266485.1:p.Cys896=
XM_005266430.3:c.2940C= XP_005266487.1:p.Cys980=
XM_005266431.2:c.2904C= XP_005266488.1:p.Cys968=
XM_005266432.2:c.2454C= XP_005266489.1:p.Cys818=
XM_006719837.2:c.2844C= XP_006719900.1:p.Cys948=
XM_006719838.1:c.756C= XP_006719901.1:p.Cys252=
XM_006719839.1:c.756C= XP_006719902.1:p.Cys252=
XM_011535117.1:c.2844C= XP_011533419.1:p.Cys948=
XM_011535118.1:c.2805C= XP_011533420.1:p.Cys935=
XM_011535119.1:c.2940C= XP_011533421.1:p.Cys980=
XM_011535120.1:c.2526C= XP_011533422.1:p.Cys842=
XM_011535121.1:c.2730+3603C= XP_011533423.1:n.2730+3603C=
XM_011535122.1:c.1608C= XP_011533424.1:p.Cys536=
XR_941601.1:n.3159C=
XR_941602.1:n.3159C=
XR_941603.1:n.3159C=
XR_941604.1:n.3159C=
NM_001330578.1:c.2706C= NP_001317507.1:p.Cys902=
NM_001330579.1:c.2688C= NP_001317508.1:p.Cys896=
XM_005266424.4:c.2844C= XP_005266481.1:p.Cys948=
XM_005266430.4:c.2940C= XP_005266487.1:p.Cys980=
XM_005266431.4:c.2904C= XP_005266488.1:p.Cys968=
XM_006719837.3:c.2844C= XP_006719900.1:p.Cys948=
XM_011535117.3:c.2844C= XP_011533419.1:p.Cys948=
XM_017020627.1:c.2844C= XP_016876116.1:p.Cys948=
NM_000053.4:c.2940C= MANE Select NP_000044.2:p.Cys980=
NM_001005918.3:c.2319C= NP_001005918.1:p.Cys773=
NM_001330579.2:c.2688C= NP_001317508.1:p.Cys896=
NM_001243182.2:c.2607C= NP_001230111.1:p.Cys869=
NM_001330578.2:c.2706C= NP_001317507.1:p.Cys902=