Canonical Allele Identifier: CA2091556946
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51939176T= , CM000675.2:g.51939176T= GRCh38
NC_000013.10:g.52513312T= , CM000675.1:g.52513312T= GRCh37
NC_000013.9:g.51411313T= NCBI36
NG_008806.1:g.77319A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1224A= ENSP00000489512.2:n.*1224A=
ENST00000673864.2:c.*2318A= ENSP00000501045.2:n.*2318A=
ENST00000674147.2:c.2953A= ENSP00000500964.2:p.Ile985=
ENST00000242839.10:c.3574A= MANE Select ENSP00000242839.5:p.Ile1192=
ENST00000344297.9:c.2953A= ENSP00000342559.5:p.Ile985=
ENST00000400366.6:c.3241A= ENSP00000383217.3:p.Ile1081=
ENST00000448424.7:c.3322A= ENSP00000416738.3:p.Ile1108=
ENST00000673696.1:n.815A=
ENST00000673772.1:c.3340A= ENSP00000501168.1:p.Ile1114=
ENST00000673867.1:n.3713A=
ENST00000673923.1:n.440A=
ENST00000674147.1:c.2509A= ENSP00000500964.1:p.Ile837=
ENST00000242839.8:c.3574A= ENSP00000242839.4:p.Ile1192=
ENST00000344297.8:c.2953A= ENSP00000342559.5:p.Ile985=
ENST00000400366.5:c.3241A= ENSP00000383217.3:p.Ile1081=
ENST00000400370.8:c.2284A= ENSP00000383221.3:p.Ile762=
ENST00000418097.7:c.3379A= ENSP00000393343.2:p.Ile1127=
ENST00000448424.6:c.3340A= ENSP00000416738.2:p.Ile1114=
ENST00000634296.1:c.1352A=
ENST00000634308.1:c.*675A= ENSP00000489234.1:n.*675A=
ENST00000634620.1:n.4318A=
ENST00000634810.1:n.2919A=
ENST00000634844.1:c.3430A= ENSP00000489398.1:p.Ile1144=
NM_000053.3:c.3574A= NP_000044.2:p.Ile1192=
NM_001005918.2:c.2953A= NP_001005918.1:p.Ile985=
NM_001243182.1:c.3241A= NP_001230111.1:p.Ile1081=
XM_005266423.2:c.3478A= XP_005266480.1:p.Ile1160=
XM_005266424.3:c.3478A= XP_005266481.1:p.Ile1160=
XM_005266427.2:c.3340A= XP_005266484.1:p.Ile1114=
XM_005266428.1:c.3322A= XP_005266485.1:p.Ile1108=
XM_005266430.3:c.3574A= XP_005266487.1:p.Ile1192=
XM_005266431.2:c.3538A= XP_005266488.1:p.Ile1180=
XM_005266432.2:c.3088A= XP_005266489.1:p.Ile1030=
XM_006719837.2:c.3478A= XP_006719900.1:p.Ile1160=
XM_006719838.1:c.1390A= XP_006719901.1:p.Ile464=
XM_006719839.1:c.1207A= XP_006719902.1:p.Ile403=
XM_011535117.1:c.3478A= XP_011533419.1:p.Ile1160=
XM_011535118.1:c.3439A= XP_011533420.1:p.Ile1147=
XM_011535119.1:c.3391A= XP_011533421.1:p.Ile1131=
XM_011535120.1:c.3160A= XP_011533422.1:p.Ile1054=
XM_011535121.1:c.3061A= XP_011533423.1:p.Ile1021=
XM_011535122.1:c.2242A= XP_011533424.1:p.Ile748=
XR_941601.1:n.3793A=
XR_941602.1:n.3793A=
XR_941603.1:n.3793A=
XR_941604.1:n.3793A=
NM_001330578.1:c.3340A= NP_001317507.1:p.Ile1114=
NM_001330579.1:c.3322A= NP_001317508.1:p.Ile1108=
XM_005266424.4:c.3478A= XP_005266481.1:p.Ile1160=
XM_005266430.4:c.3574A= XP_005266487.1:p.Ile1192=
XM_005266431.4:c.3538A= XP_005266488.1:p.Ile1180=
XM_006719837.3:c.3478A= XP_006719900.1:p.Ile1160=
XM_011535117.3:c.3478A= XP_011533419.1:p.Ile1160=
XM_017020627.1:c.3478A= XP_016876116.1:p.Ile1160=
NM_000053.4:c.3574A= MANE Select NP_000044.2:p.Ile1192=
NM_001005918.3:c.2953A= NP_001005918.1:p.Ile985=
NM_001330579.2:c.3322A= NP_001317508.1:p.Ile1108=
NM_001243182.2:c.3241A= NP_001230111.1:p.Ile1081=
NM_001330578.2:c.3340A= NP_001317507.1:p.Ile1114=