Canonical Allele Identifier: CA2091542255
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51950274G= , CM000675.2:g.51950274G= GRCh38
NC_000013.10:g.52524410G= , CM000675.1:g.52524410G= GRCh37
NC_000013.9:g.51422411G= NCBI36
NG_008806.1:g.66221C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*406C= ENSP00000489512.2:n.*406C=
ENST00000673864.2:c.*1317C= ENSP00000501045.2:n.*1317C=
ENST00000674147.2:c.2087C= ENSP00000500964.2:p.Thr696=
ENST00000242839.10:c.2573C= MANE Select ENSP00000242839.5:p.Thr858=
ENST00000344297.9:c.2087C= ENSP00000342559.5:p.Thr696=
ENST00000400366.6:c.2240C= ENSP00000383217.3:p.Thr747=
ENST00000448424.7:c.2321C= ENSP00000416738.3:p.Thr774=
ENST00000673772.1:c.2339C= ENSP00000501168.1:p.Thr780=
ENST00000674147.1:c.1643C= ENSP00000500964.1:p.Thr548=
ENST00000242839.8:c.2573C= ENSP00000242839.4:p.Thr858=
ENST00000344297.8:c.2087C= ENSP00000342559.5:p.Thr696=
ENST00000400366.5:c.2240C= ENSP00000383217.3:p.Thr747=
ENST00000400370.8:c.1286-113C= ENSP00000383221.3:n.1286-113C=
ENST00000418097.7:c.2573C= ENSP00000393343.2:p.Thr858=
ENST00000448424.6:c.2339C= ENSP00000416738.2:p.Thr780=
ENST00000634296.1:c.534C=
ENST00000634308.1:c.2339C= ENSP00000489234.1:p.Thr780=
ENST00000634620.1:n.3371C=
ENST00000634810.1:n.1918C=
ENST00000634844.1:c.2429C= ENSP00000489398.1:p.Thr810=
ENST00000635406.1:n.212-3796C=
NM_000053.3:c.2573C= NP_000044.2:p.Thr858=
NM_001005918.2:c.2087C= NP_001005918.1:p.Thr696=
NM_001243182.1:c.2240C= NP_001230111.1:p.Thr747=
XM_005266423.2:c.2477C= XP_005266480.1:p.Thr826=
XM_005266424.3:c.2477C= XP_005266481.1:p.Thr826=
XM_005266427.2:c.2339C= XP_005266484.1:p.Thr780=
XM_005266428.1:c.2321C= XP_005266485.1:p.Thr774=
XM_005266430.3:c.2573C= XP_005266487.1:p.Thr858=
XM_005266431.2:c.2537C= XP_005266488.1:p.Thr846=
XM_005266432.2:c.2087C= XP_005266489.1:p.Thr696=
XM_006719837.2:c.2477C= XP_006719900.1:p.Thr826=
XM_006719838.1:c.389C= XP_006719901.1:p.Thr130=
XM_006719839.1:c.389C= XP_006719902.1:p.Thr130=
XM_011535117.1:c.2477C= XP_011533419.1:p.Thr826=
XM_011535118.1:c.2573C= XP_011533420.1:p.Thr858=
XM_011535119.1:c.2573C= XP_011533421.1:p.Thr858=
XM_011535120.1:c.2159C= XP_011533422.1:p.Thr720=
XM_011535121.1:c.2573C= XP_011533423.1:p.Thr858=
XM_011535122.1:c.1241C= XP_011533424.1:p.Thr414=
XR_941601.1:n.2792C=
XR_941602.1:n.2792C=
XR_941603.1:n.2792C=
XR_941604.1:n.2792C=
NM_001330578.1:c.2339C= NP_001317507.1:p.Thr780=
NM_001330579.1:c.2321C= NP_001317508.1:p.Thr774=
XM_005266424.4:c.2477C= XP_005266481.1:p.Thr826=
XM_005266430.4:c.2573C= XP_005266487.1:p.Thr858=
XM_005266431.4:c.2537C= XP_005266488.1:p.Thr846=
XM_006719837.3:c.2477C= XP_006719900.1:p.Thr826=
XM_011535117.3:c.2477C= XP_011533419.1:p.Thr826=
XM_017020627.1:c.2477C= XP_016876116.1:p.Thr826=
NM_000053.4:c.2573C= MANE Select NP_000044.2:p.Thr858=
NM_001005918.3:c.2087C= NP_001005918.1:p.Thr696=
NM_001330579.2:c.2321C= NP_001317508.1:p.Thr774=
NM_001243182.2:c.2240C= NP_001230111.1:p.Thr747=
NM_001330578.2:c.2339C= NP_001317507.1:p.Thr780=