Canonical Allele Identifier: CA2091566192
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51946406A= , CM000675.2:g.51946406A= GRCh38
NC_000013.10:g.52520542A= , CM000675.1:g.52520542A= GRCh37
NC_000013.9:g.51418543A= NCBI36
NG_008806.1:g.70089T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*771T= ENSP00000489512.2:n.*771T=
ENST00000673864.2:c.*1682T= ENSP00000501045.2:n.*1682T=
ENST00000674147.2:c.2317T= ENSP00000500964.2:p.Cys773=
ENST00000242839.10:c.2938T= MANE Select ENSP00000242839.5:p.Cys980=
ENST00000344297.9:c.2317T= ENSP00000342559.5:p.Cys773=
ENST00000400366.6:c.2605T= ENSP00000383217.3:p.Cys869=
ENST00000448424.7:c.2686T= ENSP00000416738.3:p.Cys896=
ENST00000673772.1:c.2704T= ENSP00000501168.1:p.Cys902=
ENST00000673867.1:n.1085T=
ENST00000674126.1:n.3301T=
ENST00000674147.1:c.1873T= ENSP00000500964.1:p.Cys625=
ENST00000242839.8:c.2938T= ENSP00000242839.4:p.Cys980=
ENST00000344297.8:c.2317T= ENSP00000342559.5:p.Cys773=
ENST00000400366.5:c.2605T= ENSP00000383217.3:p.Cys869=
ENST00000400370.8:c.1648T= ENSP00000383221.3:p.Cys550=
ENST00000418097.7:c.2866-2115T= ENSP00000393343.2:n.2866-2115T=
ENST00000448424.6:c.2704T= ENSP00000416738.2:p.Cys902=
ENST00000466629.1:n.158T=
ENST00000634296.1:c.899T=
ENST00000634308.1:c.*39T= ENSP00000489234.1:n.*39T=
ENST00000634620.1:n.3682T=
ENST00000634810.1:n.2283T=
ENST00000634844.1:c.2794T= ENSP00000489398.1:p.Cys932=
ENST00000635406.1:n.284T=
NM_000053.3:c.2938T= NP_000044.2:p.Cys980=
NM_001005918.2:c.2317T= NP_001005918.1:p.Cys773=
NM_001243182.1:c.2605T= NP_001230111.1:p.Cys869=
XM_005266423.2:c.2842T= XP_005266480.1:p.Cys948=
XM_005266424.3:c.2842T= XP_005266481.1:p.Cys948=
XM_005266427.2:c.2704T= XP_005266484.1:p.Cys902=
XM_005266428.1:c.2686T= XP_005266485.1:p.Cys896=
XM_005266430.3:c.2938T= XP_005266487.1:p.Cys980=
XM_005266431.2:c.2902T= XP_005266488.1:p.Cys968=
XM_005266432.2:c.2452T= XP_005266489.1:p.Cys818=
XM_006719837.2:c.2842T= XP_006719900.1:p.Cys948=
XM_006719838.1:c.754T= XP_006719901.1:p.Cys252=
XM_006719839.1:c.754T= XP_006719902.1:p.Cys252=
XM_011535117.1:c.2842T= XP_011533419.1:p.Cys948=
XM_011535118.1:c.2803T= XP_011533420.1:p.Cys935=
XM_011535119.1:c.2938T= XP_011533421.1:p.Cys980=
XM_011535120.1:c.2524T= XP_011533422.1:p.Cys842=
XM_011535121.1:c.2730+3601T= XP_011533423.1:n.2730+3601T=
XM_011535122.1:c.1606T= XP_011533424.1:p.Cys536=
XR_941601.1:n.3157T=
XR_941602.1:n.3157T=
XR_941603.1:n.3157T=
XR_941604.1:n.3157T=
NM_001330578.1:c.2704T= NP_001317507.1:p.Cys902=
NM_001330579.1:c.2686T= NP_001317508.1:p.Cys896=
XM_005266424.4:c.2842T= XP_005266481.1:p.Cys948=
XM_005266430.4:c.2938T= XP_005266487.1:p.Cys980=
XM_005266431.4:c.2902T= XP_005266488.1:p.Cys968=
XM_006719837.3:c.2842T= XP_006719900.1:p.Cys948=
XM_011535117.3:c.2842T= XP_011533419.1:p.Cys948=
XM_017020627.1:c.2842T= XP_016876116.1:p.Cys948=
NM_000053.4:c.2938T= MANE Select NP_000044.2:p.Cys980=
NM_001005918.3:c.2317T= NP_001005918.1:p.Cys773=
NM_001330579.2:c.2686T= NP_001317508.1:p.Cys896=
NM_001243182.2:c.2605T= NP_001230111.1:p.Cys869=
NM_001330578.2:c.2704T= NP_001317507.1:p.Cys902=