Canonical Allele Identifier: CA2091563903
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51944183G= , CM000675.2:g.51944183G= GRCh38
NC_000013.10:g.52518319G= , CM000675.1:g.52518319G= GRCh37
NC_000013.9:g.51416320G= NCBI36
NG_008806.1:g.72312C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*894-1629C= ENSP00000489512.2:n.*894-1629C=
ENST00000673864.2:c.*1913C= ENSP00000501045.2:n.*1913C=
ENST00000674147.2:c.2548C= ENSP00000500964.2:p.Leu850=
ENST00000242839.10:c.3169C= MANE Select ENSP00000242839.5:p.Leu1057=
ENST00000344297.9:c.2548C= ENSP00000342559.5:p.Leu850=
ENST00000400366.6:c.2836C= ENSP00000383217.3:p.Leu946=
ENST00000448424.7:c.2917C= ENSP00000416738.3:p.Leu973=
ENST00000673772.1:c.2935C= ENSP00000501168.1:p.Leu979=
ENST00000673867.1:n.3308C=
ENST00000674126.1:n.3532C=
ENST00000674147.1:c.2104C= ENSP00000500964.1:p.Leu702=
ENST00000242839.8:c.3169C= ENSP00000242839.4:p.Leu1057=
ENST00000344297.8:c.2548C= ENSP00000342559.5:p.Leu850=
ENST00000400366.5:c.2836C= ENSP00000383217.3:p.Leu946=
ENST00000400370.8:c.1879C= ENSP00000383221.3:p.Leu627=
ENST00000418097.7:c.2974C= ENSP00000393343.2:p.Leu992=
ENST00000448424.6:c.2935C= ENSP00000416738.2:p.Leu979=
ENST00000466629.1:n.389C=
ENST00000634296.1:c.1022-1629C=
ENST00000634308.1:c.*270C= ENSP00000489234.1:n.*270C=
ENST00000634620.1:n.3913C=
ENST00000634810.1:n.2514C=
ENST00000634844.1:c.3025C= ENSP00000489398.1:p.Leu1009=
NM_000053.3:c.3169C= NP_000044.2:p.Leu1057=
NM_001005918.2:c.2548C= NP_001005918.1:p.Leu850=
NM_001243182.1:c.2836C= NP_001230111.1:p.Leu946=
XM_005266423.2:c.3073C= XP_005266480.1:p.Leu1025=
XM_005266424.3:c.3073C= XP_005266481.1:p.Leu1025=
XM_005266427.2:c.2935C= XP_005266484.1:p.Leu979=
XM_005266428.1:c.2917C= XP_005266485.1:p.Leu973=
XM_005266430.3:c.3169C= XP_005266487.1:p.Leu1057=
XM_005266431.2:c.3133C= XP_005266488.1:p.Leu1045=
XM_005266432.2:c.2683C= XP_005266489.1:p.Leu895=
XM_006719837.2:c.3073C= XP_006719900.1:p.Leu1025=
XM_006719838.1:c.985C= XP_006719901.1:p.Leu329=
XM_006719839.1:c.877-1629C= XP_006719902.1:n.877-1629C=
XM_011535117.1:c.3073C= XP_011533419.1:p.Leu1025=
XM_011535118.1:c.3034C= XP_011533420.1:p.Leu1012=
XM_011535119.1:c.3061-1629C= XP_011533421.1:n.3061-1629C=
XM_011535120.1:c.2755C= XP_011533422.1:p.Leu919=
XM_011535121.1:c.2731-1629C= XP_011533423.1:n.2731-1629C=
XM_011535122.1:c.1837C= XP_011533424.1:p.Leu613=
XR_941601.1:n.3388C=
XR_941602.1:n.3388C=
XR_941603.1:n.3388C=
XR_941604.1:n.3388C=
NM_001330578.1:c.2935C= NP_001317507.1:p.Leu979=
NM_001330579.1:c.2917C= NP_001317508.1:p.Leu973=
XM_005266424.4:c.3073C= XP_005266481.1:p.Leu1025=
XM_005266430.4:c.3169C= XP_005266487.1:p.Leu1057=
XM_005266431.4:c.3133C= XP_005266488.1:p.Leu1045=
XM_006719837.3:c.3073C= XP_006719900.1:p.Leu1025=
XM_011535117.3:c.3073C= XP_011533419.1:p.Leu1025=
XM_017020627.1:c.3073C= XP_016876116.1:p.Leu1025=
NM_000053.4:c.3169C= MANE Select NP_000044.2:p.Leu1057=
NM_001005918.3:c.2548C= NP_001005918.1:p.Leu850=
NM_001330579.2:c.2917C= NP_001317508.1:p.Leu973=
NM_001243182.2:c.2836C= NP_001230111.1:p.Leu946=
NM_001330578.2:c.2935C= NP_001317507.1:p.Leu979=