Canonical Allele Identifier: CA2091563873
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51944171C= , CM000675.2:g.51944171C= GRCh38
NC_000013.10:g.52518307C= , CM000675.1:g.52518307C= GRCh37
NC_000013.9:g.51416308C= NCBI36
NG_008806.1:g.72324G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*894-1617G= ENSP00000489512.2:n.*894-1617G=
ENST00000673864.2:c.*1925G= ENSP00000501045.2:n.*1925G=
ENST00000674147.2:c.2560G= ENSP00000500964.2:p.Gly854=
ENST00000242839.10:c.3181G= MANE Select ENSP00000242839.5:p.Gly1061=
ENST00000344297.9:c.2560G= ENSP00000342559.5:p.Gly854=
ENST00000400366.6:c.2848G= ENSP00000383217.3:p.Gly950=
ENST00000448424.7:c.2929G= ENSP00000416738.3:p.Gly977=
ENST00000673772.1:c.2947G= ENSP00000501168.1:p.Gly983=
ENST00000673867.1:n.3320G=
ENST00000674126.1:n.3544G=
ENST00000674147.1:c.2116G= ENSP00000500964.1:p.Gly706=
ENST00000242839.8:c.3181G= ENSP00000242839.4:p.Gly1061=
ENST00000344297.8:c.2560G= ENSP00000342559.5:p.Gly854=
ENST00000400366.5:c.2848G= ENSP00000383217.3:p.Gly950=
ENST00000400370.8:c.1891G= ENSP00000383221.3:p.Gly631=
ENST00000418097.7:c.2986G= ENSP00000393343.2:p.Gly996=
ENST00000448424.6:c.2947G= ENSP00000416738.2:p.Gly983=
ENST00000466629.1:n.401G=
ENST00000634296.1:c.1022-1617G=
ENST00000634308.1:c.*282G= ENSP00000489234.1:n.*282G=
ENST00000634620.1:n.3925G=
ENST00000634810.1:n.2526G=
ENST00000634844.1:c.3037G= ENSP00000489398.1:p.Gly1013=
NM_000053.3:c.3181G= NP_000044.2:p.Gly1061=
NM_001005918.2:c.2560G= NP_001005918.1:p.Gly854=
NM_001243182.1:c.2848G= NP_001230111.1:p.Gly950=
XM_005266423.2:c.3085G= XP_005266480.1:p.Gly1029=
XM_005266424.3:c.3085G= XP_005266481.1:p.Gly1029=
XM_005266427.2:c.2947G= XP_005266484.1:p.Gly983=
XM_005266428.1:c.2929G= XP_005266485.1:p.Gly977=
XM_005266430.3:c.3181G= XP_005266487.1:p.Gly1061=
XM_005266431.2:c.3145G= XP_005266488.1:p.Gly1049=
XM_005266432.2:c.2695G= XP_005266489.1:p.Gly899=
XM_006719837.2:c.3085G= XP_006719900.1:p.Gly1029=
XM_006719838.1:c.997G= XP_006719901.1:p.Gly333=
XM_006719839.1:c.877-1617G= XP_006719902.1:n.877-1617G=
XM_011535117.1:c.3085G= XP_011533419.1:p.Gly1029=
XM_011535118.1:c.3046G= XP_011533420.1:p.Gly1016=
XM_011535119.1:c.3061-1617G= XP_011533421.1:n.3061-1617G=
XM_011535120.1:c.2767G= XP_011533422.1:p.Gly923=
XM_011535121.1:c.2731-1617G= XP_011533423.1:n.2731-1617G=
XM_011535122.1:c.1849G= XP_011533424.1:p.Gly617=
XR_941601.1:n.3400G=
XR_941602.1:n.3400G=
XR_941603.1:n.3400G=
XR_941604.1:n.3400G=
NM_001330578.1:c.2947G= NP_001317507.1:p.Gly983=
NM_001330579.1:c.2929G= NP_001317508.1:p.Gly977=
XM_005266424.4:c.3085G= XP_005266481.1:p.Gly1029=
XM_005266430.4:c.3181G= XP_005266487.1:p.Gly1061=
XM_005266431.4:c.3145G= XP_005266488.1:p.Gly1049=
XM_006719837.3:c.3085G= XP_006719900.1:p.Gly1029=
XM_011535117.3:c.3085G= XP_011533419.1:p.Gly1029=
XM_017020627.1:c.3085G= XP_016876116.1:p.Gly1029=
NM_000053.4:c.3181G= MANE Select NP_000044.2:p.Gly1061=
NM_001005918.3:c.2560G= NP_001005918.1:p.Gly854=
NM_001330579.2:c.2929G= NP_001317508.1:p.Gly977=
NM_001243182.2:c.2848G= NP_001230111.1:p.Gly950=
NM_001330578.2:c.2947G= NP_001317507.1:p.Gly983=