Canonical Allele Identifier: CA2091542277
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51950286T= , CM000675.2:g.51950286T= GRCh38
NC_000013.10:g.52524422T= , CM000675.1:g.52524422T= GRCh37
NC_000013.9:g.51422423T= NCBI36
NG_008806.1:g.66209A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*394A= ENSP00000489512.2:n.*394A=
ENST00000673864.2:c.*1305A= ENSP00000501045.2:n.*1305A=
ENST00000674147.2:c.2075A= ENSP00000500964.2:p.Glu692=
ENST00000242839.10:c.2561A= MANE Select ENSP00000242839.5:p.Glu854=
ENST00000344297.9:c.2075A= ENSP00000342559.5:p.Glu692=
ENST00000400366.6:c.2228A= ENSP00000383217.3:p.Glu743=
ENST00000448424.7:c.2309A= ENSP00000416738.3:p.Glu770=
ENST00000673772.1:c.2327A= ENSP00000501168.1:p.Glu776=
ENST00000674147.1:c.1631A= ENSP00000500964.1:p.Glu544=
ENST00000242839.8:c.2561A= ENSP00000242839.4:p.Glu854=
ENST00000344297.8:c.2075A= ENSP00000342559.5:p.Glu692=
ENST00000400366.5:c.2228A= ENSP00000383217.3:p.Glu743=
ENST00000400370.8:c.1286-125A= ENSP00000383221.3:n.1286-125A=
ENST00000418097.7:c.2561A= ENSP00000393343.2:p.Glu854=
ENST00000448424.6:c.2327A= ENSP00000416738.2:p.Glu776=
ENST00000634296.1:c.522A=
ENST00000634308.1:c.2327A= ENSP00000489234.1:p.Glu776=
ENST00000634620.1:n.3359A=
ENST00000634810.1:n.1906A=
ENST00000634844.1:c.2417A= ENSP00000489398.1:p.Glu806=
ENST00000635406.1:n.212-3808A=
NM_000053.3:c.2561A= NP_000044.2:p.Glu854=
NM_001005918.2:c.2075A= NP_001005918.1:p.Glu692=
NM_001243182.1:c.2228A= NP_001230111.1:p.Glu743=
XM_005266423.2:c.2465A= XP_005266480.1:p.Glu822=
XM_005266424.3:c.2465A= XP_005266481.1:p.Glu822=
XM_005266427.2:c.2327A= XP_005266484.1:p.Glu776=
XM_005266428.1:c.2309A= XP_005266485.1:p.Glu770=
XM_005266430.3:c.2561A= XP_005266487.1:p.Glu854=
XM_005266431.2:c.2525A= XP_005266488.1:p.Glu842=
XM_005266432.2:c.2075A= XP_005266489.1:p.Glu692=
XM_006719837.2:c.2465A= XP_006719900.1:p.Glu822=
XM_006719838.1:c.377A= XP_006719901.1:p.Glu126=
XM_006719839.1:c.377A= XP_006719902.1:p.Glu126=
XM_011535117.1:c.2465A= XP_011533419.1:p.Glu822=
XM_011535118.1:c.2561A= XP_011533420.1:p.Glu854=
XM_011535119.1:c.2561A= XP_011533421.1:p.Glu854=
XM_011535120.1:c.2147A= XP_011533422.1:p.Glu716=
XM_011535121.1:c.2561A= XP_011533423.1:p.Glu854=
XM_011535122.1:c.1229A= XP_011533424.1:p.Glu410=
XR_941601.1:n.2780A=
XR_941602.1:n.2780A=
XR_941603.1:n.2780A=
XR_941604.1:n.2780A=
NM_001330578.1:c.2327A= NP_001317507.1:p.Glu776=
NM_001330579.1:c.2309A= NP_001317508.1:p.Glu770=
XM_005266424.4:c.2465A= XP_005266481.1:p.Glu822=
XM_005266430.4:c.2561A= XP_005266487.1:p.Glu854=
XM_005266431.4:c.2525A= XP_005266488.1:p.Glu842=
XM_006719837.3:c.2465A= XP_006719900.1:p.Glu822=
XM_011535117.3:c.2465A= XP_011533419.1:p.Glu822=
XM_017020627.1:c.2465A= XP_016876116.1:p.Glu822=
NM_000053.4:c.2561A= MANE Select NP_000044.2:p.Glu854=
NM_001005918.3:c.2075A= NP_001005918.1:p.Glu692=
NM_001330579.2:c.2309A= NP_001317508.1:p.Glu770=
NM_001243182.2:c.2228A= NP_001230111.1:p.Glu743=
NM_001330578.2:c.2327A= NP_001317507.1:p.Glu776=