Canonical Allele Identifier: CA2091553488
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51937353T= , CM000675.2:g.51937353T= GRCh38
NC_000013.10:g.52511489T= , CM000675.1:g.52511489T= GRCh37
NC_000013.9:g.51409490T= NCBI36
NG_008806.1:g.79142A=

Transcript Alleles

HGVS Amino-acid change
ENST00000634296.2:c.*1594A= ENSP00000489512.2:n.*1594A=
ENST00000673864.2:c.*2688A= ENSP00000501045.2:n.*2688A=
ENST00000674147.2:c.3323A= ENSP00000500964.2:p.Lys1108=
ENST00000242839.10:c.3944A= MANE Select ENSP00000242839.5:p.Lys1315=
ENST00000344297.9:c.3323A= ENSP00000342559.5:p.Lys1108=
ENST00000400366.6:c.3611A= ENSP00000383217.3:p.Lys1204=
ENST00000448424.7:c.3692A= ENSP00000416738.3:p.Lys1231=
ENST00000673696.1:n.1267A=
ENST00000673772.1:c.3710A= ENSP00000501168.1:p.Lys1237=
ENST00000673867.1:n.4083A=
ENST00000673923.1:n.810A=
ENST00000674147.1:c.2879A= ENSP00000500964.1:p.Lys960=
ENST00000242839.8:c.3944A= ENSP00000242839.4:p.Lys1315=
ENST00000344297.8:c.3323A= ENSP00000342559.5:p.Lys1108=
ENST00000400366.5:c.3611A= ENSP00000383217.3:p.Lys1204=
ENST00000400370.8:c.2654A= ENSP00000383221.3:p.Lys885=
ENST00000418097.7:c.3749A= ENSP00000393343.2:p.Lys1250=
ENST00000448424.6:c.3710A= ENSP00000416738.2:p.Lys1237=
ENST00000634296.1:c.1722A=
ENST00000634308.1:c.*1045A= ENSP00000489234.1:n.*1045A=
ENST00000634620.1:n.4688A=
ENST00000634810.1:n.3289A=
ENST00000634844.1:c.3800A= ENSP00000489398.1:p.Lys1267=
NM_000053.3:c.3944A= NP_000044.2:p.Lys1315=
NM_001005918.2:c.3323A= NP_001005918.1:p.Lys1108=
NM_001243182.1:c.3611A= NP_001230111.1:p.Lys1204=
XM_005266423.2:c.3848A= XP_005266480.1:p.Lys1283=
XM_005266424.3:c.3848A= XP_005266481.1:p.Lys1283=
XM_005266427.2:c.3710A= XP_005266484.1:p.Lys1237=
XM_005266428.1:c.3692A= XP_005266485.1:p.Lys1231=
XM_005266430.3:c.3944A= XP_005266487.1:p.Lys1315=
XM_005266431.2:c.3908A= XP_005266488.1:p.Lys1303=
XM_005266432.2:c.3458A= XP_005266489.1:p.Lys1153=
XM_006719837.2:c.3848A= XP_006719900.1:p.Lys1283=
XM_006719838.1:c.1760A= XP_006719901.1:p.Lys587=
XM_006719839.1:c.1577A= XP_006719902.1:p.Lys526=
XM_011535117.1:c.3848A= XP_011533419.1:p.Lys1283=
XM_011535118.1:c.3809A= XP_011533420.1:p.Lys1270=
XM_011535119.1:c.3761A= XP_011533421.1:p.Lys1254=
XM_011535120.1:c.3530A= XP_011533422.1:p.Lys1177=
XM_011535121.1:c.3431A= XP_011533423.1:p.Lys1144=
XM_011535122.1:c.2612A= XP_011533424.1:p.Lys871=
XR_941601.1:n.4163A=
XR_941602.1:n.4163A=
XR_941603.1:n.4163A=
XR_941604.1:n.4163A=
NM_001330578.1:c.3710A= NP_001317507.1:p.Lys1237=
NM_001330579.1:c.3692A= NP_001317508.1:p.Lys1231=
XM_005266424.4:c.3848A= XP_005266481.1:p.Lys1283=
XM_005266430.4:c.3944A= XP_005266487.1:p.Lys1315=
XM_005266431.4:c.3908A= XP_005266488.1:p.Lys1303=
XM_006719837.3:c.3848A= XP_006719900.1:p.Lys1283=
XM_011535117.3:c.3848A= XP_011533419.1:p.Lys1283=
XM_017020627.1:c.3848A= XP_016876116.1:p.Lys1283=
NM_000053.4:c.3944A= MANE Select NP_000044.2:p.Lys1315=
NM_001005918.3:c.3323A= NP_001005918.1:p.Lys1108=
NM_001330579.2:c.3692A= NP_001317508.1:p.Lys1231=
NM_001243182.2:c.3611A= NP_001230111.1:p.Lys1204=
NM_001330578.2:c.3710A= NP_001317507.1:p.Lys1237=