Canonical Allele Identifier: CA2091563914
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51944189T= , CM000675.2:g.51944189T= GRCh38
NC_000013.10:g.52518325T= , CM000675.1:g.52518325T= GRCh37
NC_000013.9:g.51416326T= NCBI36
NG_008806.1:g.72306A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*894-1635A= ENSP00000489512.2:n.*894-1635A=
ENST00000673864.2:c.*1907A= ENSP00000501045.2:n.*1907A=
ENST00000674147.2:c.2542A= ENSP00000500964.2:p.Lys848=
ENST00000242839.10:c.3163A= MANE Select ENSP00000242839.5:p.Lys1055=
ENST00000344297.9:c.2542A= ENSP00000342559.5:p.Lys848=
ENST00000400366.6:c.2830A= ENSP00000383217.3:p.Lys944=
ENST00000448424.7:c.2911A= ENSP00000416738.3:p.Lys971=
ENST00000673772.1:c.2929A= ENSP00000501168.1:p.Lys977=
ENST00000673867.1:n.3302A=
ENST00000674126.1:n.3526A=
ENST00000674147.1:c.2098A= ENSP00000500964.1:p.Lys700=
ENST00000242839.8:c.3163A= ENSP00000242839.4:p.Lys1055=
ENST00000344297.8:c.2542A= ENSP00000342559.5:p.Lys848=
ENST00000400366.5:c.2830A= ENSP00000383217.3:p.Lys944=
ENST00000400370.8:c.1873A= ENSP00000383221.3:p.Lys625=
ENST00000418097.7:c.2968A= ENSP00000393343.2:p.Lys990=
ENST00000448424.6:c.2929A= ENSP00000416738.2:p.Lys977=
ENST00000466629.1:n.383A=
ENST00000634296.1:c.1022-1635A=
ENST00000634308.1:c.*264A= ENSP00000489234.1:n.*264A=
ENST00000634620.1:n.3907A=
ENST00000634810.1:n.2508A=
ENST00000634844.1:c.3019A= ENSP00000489398.1:p.Lys1007=
NM_000053.3:c.3163A= NP_000044.2:p.Lys1055=
NM_001005918.2:c.2542A= NP_001005918.1:p.Lys848=
NM_001243182.1:c.2830A= NP_001230111.1:p.Lys944=
XM_005266423.2:c.3067A= XP_005266480.1:p.Lys1023=
XM_005266424.3:c.3067A= XP_005266481.1:p.Lys1023=
XM_005266427.2:c.2929A= XP_005266484.1:p.Lys977=
XM_005266428.1:c.2911A= XP_005266485.1:p.Lys971=
XM_005266430.3:c.3163A= XP_005266487.1:p.Lys1055=
XM_005266431.2:c.3127A= XP_005266488.1:p.Lys1043=
XM_005266432.2:c.2677A= XP_005266489.1:p.Lys893=
XM_006719837.2:c.3067A= XP_006719900.1:p.Lys1023=
XM_006719838.1:c.979A= XP_006719901.1:p.Lys327=
XM_006719839.1:c.877-1635A= XP_006719902.1:n.877-1635A=
XM_011535117.1:c.3067A= XP_011533419.1:p.Lys1023=
XM_011535118.1:c.3028A= XP_011533420.1:p.Lys1010=
XM_011535119.1:c.3061-1635A= XP_011533421.1:n.3061-1635A=
XM_011535120.1:c.2749A= XP_011533422.1:p.Lys917=
XM_011535121.1:c.2731-1635A= XP_011533423.1:n.2731-1635A=
XM_011535122.1:c.1831A= XP_011533424.1:p.Lys611=
XR_941601.1:n.3382A=
XR_941602.1:n.3382A=
XR_941603.1:n.3382A=
XR_941604.1:n.3382A=
NM_001330578.1:c.2929A= NP_001317507.1:p.Lys977=
NM_001330579.1:c.2911A= NP_001317508.1:p.Lys971=
XM_005266424.4:c.3067A= XP_005266481.1:p.Lys1023=
XM_005266430.4:c.3163A= XP_005266487.1:p.Lys1055=
XM_005266431.4:c.3127A= XP_005266488.1:p.Lys1043=
XM_006719837.3:c.3067A= XP_006719900.1:p.Lys1023=
XM_011535117.3:c.3067A= XP_011533419.1:p.Lys1023=
XM_017020627.1:c.3067A= XP_016876116.1:p.Lys1023=
NM_000053.4:c.3163A= MANE Select NP_000044.2:p.Lys1055=
NM_001005918.3:c.2542A= NP_001005918.1:p.Lys848=
NM_001330579.2:c.2911A= NP_001317508.1:p.Lys971=
NM_001243182.2:c.2830A= NP_001230111.1:p.Lys944=
NM_001330578.2:c.2929A= NP_001317507.1:p.Lys977=