Canonical Allele Identifier: CA2091556957
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51939181C= , CM000675.2:g.51939181C= GRCh38
NC_000013.10:g.52513317C= , CM000675.1:g.52513317C= GRCh37
NC_000013.9:g.51411318C= NCBI36
NG_008806.1:g.77314G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1219G= ENSP00000489512.2:n.*1219G=
ENST00000673864.2:c.*2313G= ENSP00000501045.2:n.*2313G=
ENST00000674147.2:c.2948G= ENSP00000500964.2:p.Gly983=
ENST00000242839.10:c.3569G= MANE Select ENSP00000242839.5:p.Gly1190=
ENST00000344297.9:c.2948G= ENSP00000342559.5:p.Gly983=
ENST00000400366.6:c.3236G= ENSP00000383217.3:p.Gly1079=
ENST00000448424.7:c.3317G= ENSP00000416738.3:p.Gly1106=
ENST00000673696.1:n.810G=
ENST00000673772.1:c.3335G= ENSP00000501168.1:p.Gly1112=
ENST00000673867.1:n.3708G=
ENST00000673923.1:n.435G=
ENST00000674147.1:c.2504G= ENSP00000500964.1:p.Gly835=
ENST00000242839.8:c.3569G= ENSP00000242839.4:p.Gly1190=
ENST00000344297.8:c.2948G= ENSP00000342559.5:p.Gly983=
ENST00000400366.5:c.3236G= ENSP00000383217.3:p.Gly1079=
ENST00000400370.8:c.2279G= ENSP00000383221.3:p.Gly760=
ENST00000418097.7:c.3374G= ENSP00000393343.2:p.Gly1125=
ENST00000448424.6:c.3335G= ENSP00000416738.2:p.Gly1112=
ENST00000634296.1:c.1347G=
ENST00000634308.1:c.*670G= ENSP00000489234.1:n.*670G=
ENST00000634620.1:n.4313G=
ENST00000634810.1:n.2914G=
ENST00000634844.1:c.3425G= ENSP00000489398.1:p.Gly1142=
NM_000053.3:c.3569G= NP_000044.2:p.Gly1190=
NM_001005918.2:c.2948G= NP_001005918.1:p.Gly983=
NM_001243182.1:c.3236G= NP_001230111.1:p.Gly1079=
XM_005266423.2:c.3473G= XP_005266480.1:p.Gly1158=
XM_005266424.3:c.3473G= XP_005266481.1:p.Gly1158=
XM_005266427.2:c.3335G= XP_005266484.1:p.Gly1112=
XM_005266428.1:c.3317G= XP_005266485.1:p.Gly1106=
XM_005266430.3:c.3569G= XP_005266487.1:p.Gly1190=
XM_005266431.2:c.3533G= XP_005266488.1:p.Gly1178=
XM_005266432.2:c.3083G= XP_005266489.1:p.Gly1028=
XM_006719837.2:c.3473G= XP_006719900.1:p.Gly1158=
XM_006719838.1:c.1385G= XP_006719901.1:p.Gly462=
XM_006719839.1:c.1202G= XP_006719902.1:p.Gly401=
XM_011535117.1:c.3473G= XP_011533419.1:p.Gly1158=
XM_011535118.1:c.3434G= XP_011533420.1:p.Gly1145=
XM_011535119.1:c.3386G= XP_011533421.1:p.Gly1129=
XM_011535120.1:c.3155G= XP_011533422.1:p.Gly1052=
XM_011535121.1:c.3056G= XP_011533423.1:p.Gly1019=
XM_011535122.1:c.2237G= XP_011533424.1:p.Gly746=
XR_941601.1:n.3788G=
XR_941602.1:n.3788G=
XR_941603.1:n.3788G=
XR_941604.1:n.3788G=
NM_001330578.1:c.3335G= NP_001317507.1:p.Gly1112=
NM_001330579.1:c.3317G= NP_001317508.1:p.Gly1106=
XM_005266424.4:c.3473G= XP_005266481.1:p.Gly1158=
XM_005266430.4:c.3569G= XP_005266487.1:p.Gly1190=
XM_005266431.4:c.3533G= XP_005266488.1:p.Gly1178=
XM_006719837.3:c.3473G= XP_006719900.1:p.Gly1158=
XM_011535117.3:c.3473G= XP_011533419.1:p.Gly1158=
XM_017020627.1:c.3473G= XP_016876116.1:p.Gly1158=
NM_000053.4:c.3569G= MANE Select NP_000044.2:p.Gly1190=
NM_001005918.3:c.2948G= NP_001005918.1:p.Gly983=
NM_001330579.2:c.3317G= NP_001317508.1:p.Gly1106=
NM_001243182.2:c.3236G= NP_001230111.1:p.Gly1079=
NM_001330578.2:c.3335G= NP_001317507.1:p.Gly1112=