Canonical Allele Identifier: CA2091553310
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51937285T= , CM000675.2:g.51937285T= GRCh38
NC_000013.10:g.52511421T= , CM000675.1:g.52511421T= GRCh37
NC_000013.9:g.51409422T= NCBI36
NG_008806.1:g.79210A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1662A= ENSP00000489512.2:n.*1662A=
ENST00000673864.2:c.*2756A= ENSP00000501045.2:n.*2756A=
ENST00000674147.2:c.3391A= ENSP00000500964.2:p.Ile1131=
ENST00000242839.10:c.4012A= MANE Select ENSP00000242839.5:p.Ile1338=
ENST00000344297.9:c.3391A= ENSP00000342559.5:p.Ile1131=
ENST00000400366.6:c.3679A= ENSP00000383217.3:p.Ile1227=
ENST00000448424.7:c.3760A= ENSP00000416738.3:p.Ile1254=
ENST00000673696.1:n.1335A=
ENST00000673772.1:c.3778A= ENSP00000501168.1:p.Ile1260=
ENST00000673867.1:n.4151A=
ENST00000673923.1:n.878A=
ENST00000674147.1:c.2947A= ENSP00000500964.1:p.Ile983=
ENST00000242839.8:c.4012A= ENSP00000242839.4:p.Ile1338=
ENST00000344297.8:c.3391A= ENSP00000342559.5:p.Ile1131=
ENST00000400366.5:c.3679A= ENSP00000383217.3:p.Ile1227=
ENST00000400370.8:c.2722A= ENSP00000383221.3:p.Ile908=
ENST00000418097.7:c.3817A= ENSP00000393343.2:p.Ile1273=
ENST00000448424.6:c.3778A= ENSP00000416738.2:p.Ile1260=
ENST00000634296.1:c.1790A=
ENST00000634308.1:c.*1113A= ENSP00000489234.1:n.*1113A=
ENST00000634620.1:n.4756A=
ENST00000634810.1:n.3357A=
ENST00000634844.1:c.3868A= ENSP00000489398.1:p.Ile1290=
NM_000053.3:c.4012A= NP_000044.2:p.Ile1338=
NM_001005918.2:c.3391A= NP_001005918.1:p.Ile1131=
NM_001243182.1:c.3679A= NP_001230111.1:p.Ile1227=
XM_005266423.2:c.3916A= XP_005266480.1:p.Ile1306=
XM_005266424.3:c.3916A= XP_005266481.1:p.Ile1306=
XM_005266427.2:c.3778A= XP_005266484.1:p.Ile1260=
XM_005266428.1:c.3760A= XP_005266485.1:p.Ile1254=
XM_005266430.3:c.4012A= XP_005266487.1:p.Ile1338=
XM_005266431.2:c.3976A= XP_005266488.1:p.Ile1326=
XM_005266432.2:c.3526A= XP_005266489.1:p.Ile1176=
XM_006719837.2:c.3916A= XP_006719900.1:p.Ile1306=
XM_006719838.1:c.1828A= XP_006719901.1:p.Ile610=
XM_006719839.1:c.1645A= XP_006719902.1:p.Ile549=
XM_011535117.1:c.3916A= XP_011533419.1:p.Ile1306=
XM_011535118.1:c.3877A= XP_011533420.1:p.Ile1293=
XM_011535119.1:c.3829A= XP_011533421.1:p.Ile1277=
XM_011535120.1:c.3598A= XP_011533422.1:p.Ile1200=
XM_011535121.1:c.3499A= XP_011533423.1:p.Ile1167=
XM_011535122.1:c.2680A= XP_011533424.1:p.Ile894=
XR_941601.1:n.4231A=
XR_941602.1:n.4231A=
XR_941603.1:n.4231A=
XR_941604.1:n.4231A=
NM_001330578.1:c.3778A= NP_001317507.1:p.Ile1260=
NM_001330579.1:c.3760A= NP_001317508.1:p.Ile1254=
XM_005266424.4:c.3916A= XP_005266481.1:p.Ile1306=
XM_005266430.4:c.4012A= XP_005266487.1:p.Ile1338=
XM_005266431.4:c.3976A= XP_005266488.1:p.Ile1326=
XM_006719837.3:c.3916A= XP_006719900.1:p.Ile1306=
XM_011535117.3:c.3916A= XP_011533419.1:p.Ile1306=
XM_017020627.1:c.3916A= XP_016876116.1:p.Ile1306=
NM_000053.4:c.4012A= MANE Select NP_000044.2:p.Ile1338=
NM_001005918.3:c.3391A= NP_001005918.1:p.Ile1131=
NM_001330579.2:c.3760A= NP_001317508.1:p.Ile1254=
NM_001243182.2:c.3679A= NP_001230111.1:p.Ile1227=
NM_001330578.2:c.3778A= NP_001317507.1:p.Ile1260=