Canonical Allele Identifier: CA2091542536
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51950392G= , CM000675.2:g.51950392G= GRCh38
NC_000013.10:g.52524528G= , CM000675.1:g.52524528G= GRCh37
NC_000013.9:g.51422529G= NCBI36
NG_008806.1:g.66103C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*288C= ENSP00000489512.2:n.*288C=
ENST00000673864.2:c.*1199C= ENSP00000501045.2:n.*1199C=
ENST00000674147.2:c.1969C= ENSP00000500964.2:p.Gln657=
ENST00000242839.10:c.2455C= MANE Select ENSP00000242839.5:p.Gln819=
ENST00000344297.9:c.1969C= ENSP00000342559.5:p.Gln657=
ENST00000400366.6:c.2122C= ENSP00000383217.3:p.Gln708=
ENST00000448424.7:c.2203C= ENSP00000416738.3:p.Gln735=
ENST00000673772.1:c.2221C= ENSP00000501168.1:p.Gln741=
ENST00000674147.1:c.1525C= ENSP00000500964.1:p.Gln509=
ENST00000242839.8:c.2455C= ENSP00000242839.4:p.Gln819=
ENST00000344297.8:c.1969C= ENSP00000342559.5:p.Gln657=
ENST00000400366.5:c.2122C= ENSP00000383217.3:p.Gln708=
ENST00000400370.8:c.1286-231C= ENSP00000383221.3:n.1286-231C=
ENST00000418097.7:c.2455C= ENSP00000393343.2:p.Gln819=
ENST00000448424.6:c.2221C= ENSP00000416738.2:p.Gln741=
ENST00000634296.1:c.416C=
ENST00000634308.1:c.2221C= ENSP00000489234.1:p.Gln741=
ENST00000634620.1:n.3253C=
ENST00000634810.1:n.1800C=
ENST00000634844.1:c.2311C= ENSP00000489398.1:p.Gln771=
ENST00000635406.1:n.212-3914C=
NM_000053.3:c.2455C= NP_000044.2:p.Gln819=
NM_001005918.2:c.1969C= NP_001005918.1:p.Gln657=
NM_001243182.1:c.2122C= NP_001230111.1:p.Gln708=
XM_005266423.2:c.2359C= XP_005266480.1:p.Gln787=
XM_005266424.3:c.2359C= XP_005266481.1:p.Gln787=
XM_005266427.2:c.2221C= XP_005266484.1:p.Gln741=
XM_005266428.1:c.2203C= XP_005266485.1:p.Gln735=
XM_005266430.3:c.2455C= XP_005266487.1:p.Gln819=
XM_005266431.2:c.2419C= XP_005266488.1:p.Gln807=
XM_005266432.2:c.1969C= XP_005266489.1:p.Gln657=
XM_006719837.2:c.2359C= XP_006719900.1:p.Gln787=
XM_006719838.1:c.271C= XP_006719901.1:p.Gln91=
XM_006719839.1:c.271C= XP_006719902.1:p.Gln91=
XM_011535117.1:c.2359C= XP_011533419.1:p.Gln787=
XM_011535118.1:c.2455C= XP_011533420.1:p.Gln819=
XM_011535119.1:c.2455C= XP_011533421.1:p.Gln819=
XM_011535120.1:c.2041C= XP_011533422.1:p.Gln681=
XM_011535121.1:c.2455C= XP_011533423.1:p.Gln819=
XM_011535122.1:c.1123C= XP_011533424.1:p.Gln375=
XR_941601.1:n.2674C=
XR_941602.1:n.2674C=
XR_941603.1:n.2674C=
XR_941604.1:n.2674C=
NM_001330578.1:c.2221C= NP_001317507.1:p.Gln741=
NM_001330579.1:c.2203C= NP_001317508.1:p.Gln735=
XM_005266424.4:c.2359C= XP_005266481.1:p.Gln787=
XM_005266430.4:c.2455C= XP_005266487.1:p.Gln819=
XM_005266431.4:c.2419C= XP_005266488.1:p.Gln807=
XM_006719837.3:c.2359C= XP_006719900.1:p.Gln787=
XM_011535117.3:c.2359C= XP_011533419.1:p.Gln787=
XM_017020627.1:c.2359C= XP_016876116.1:p.Gln787=
NM_000053.4:c.2455C= MANE Select NP_000044.2:p.Gln819=
NM_001005918.3:c.1969C= NP_001005918.1:p.Gln657=
NM_001330579.2:c.2203C= NP_001317508.1:p.Gln735=
NM_001243182.2:c.2122C= NP_001230111.1:p.Gln708=
NM_001330578.2:c.2221C= NP_001317507.1:p.Gln741=