Canonical Allele Identifier: CA2091542507
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51950380C= , CM000675.2:g.51950380C= GRCh38
NC_000013.10:g.52524516C= , CM000675.1:g.52524516C= GRCh37
NC_000013.9:g.51422517C= NCBI36
NG_008806.1:g.66115G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*300G= ENSP00000489512.2:n.*300G=
ENST00000673864.2:c.*1211G= ENSP00000501045.2:n.*1211G=
ENST00000674147.2:c.1981G= ENSP00000500964.2:p.Glu661=
ENST00000242839.10:c.2467G= MANE Select ENSP00000242839.5:p.Glu823=
ENST00000344297.9:c.1981G= ENSP00000342559.5:p.Glu661=
ENST00000400366.6:c.2134G= ENSP00000383217.3:p.Glu712=
ENST00000448424.7:c.2215G= ENSP00000416738.3:p.Glu739=
ENST00000673772.1:c.2233G= ENSP00000501168.1:p.Glu745=
ENST00000674147.1:c.1537G= ENSP00000500964.1:p.Glu513=
ENST00000242839.8:c.2467G= ENSP00000242839.4:p.Glu823=
ENST00000344297.8:c.1981G= ENSP00000342559.5:p.Glu661=
ENST00000400366.5:c.2134G= ENSP00000383217.3:p.Glu712=
ENST00000400370.8:c.1286-219G= ENSP00000383221.3:n.1286-219G=
ENST00000418097.7:c.2467G= ENSP00000393343.2:p.Glu823=
ENST00000448424.6:c.2233G= ENSP00000416738.2:p.Glu745=
ENST00000634296.1:c.428G=
ENST00000634308.1:c.2233G= ENSP00000489234.1:p.Glu745=
ENST00000634620.1:n.3265G=
ENST00000634810.1:n.1812G=
ENST00000634844.1:c.2323G= ENSP00000489398.1:p.Glu775=
ENST00000635406.1:n.212-3902G=
NM_000053.3:c.2467G= NP_000044.2:p.Glu823=
NM_001005918.2:c.1981G= NP_001005918.1:p.Glu661=
NM_001243182.1:c.2134G= NP_001230111.1:p.Glu712=
XM_005266423.2:c.2371G= XP_005266480.1:p.Glu791=
XM_005266424.3:c.2371G= XP_005266481.1:p.Glu791=
XM_005266427.2:c.2233G= XP_005266484.1:p.Glu745=
XM_005266428.1:c.2215G= XP_005266485.1:p.Glu739=
XM_005266430.3:c.2467G= XP_005266487.1:p.Glu823=
XM_005266431.2:c.2431G= XP_005266488.1:p.Glu811=
XM_005266432.2:c.1981G= XP_005266489.1:p.Glu661=
XM_006719837.2:c.2371G= XP_006719900.1:p.Glu791=
XM_006719838.1:c.283G= XP_006719901.1:p.Glu95=
XM_006719839.1:c.283G= XP_006719902.1:p.Glu95=
XM_011535117.1:c.2371G= XP_011533419.1:p.Glu791=
XM_011535118.1:c.2467G= XP_011533420.1:p.Glu823=
XM_011535119.1:c.2467G= XP_011533421.1:p.Glu823=
XM_011535120.1:c.2053G= XP_011533422.1:p.Glu685=
XM_011535121.1:c.2467G= XP_011533423.1:p.Glu823=
XM_011535122.1:c.1135G= XP_011533424.1:p.Glu379=
XR_941601.1:n.2686G=
XR_941602.1:n.2686G=
XR_941603.1:n.2686G=
XR_941604.1:n.2686G=
NM_001330578.1:c.2233G= NP_001317507.1:p.Glu745=
NM_001330579.1:c.2215G= NP_001317508.1:p.Glu739=
XM_005266424.4:c.2371G= XP_005266481.1:p.Glu791=
XM_005266430.4:c.2467G= XP_005266487.1:p.Glu823=
XM_005266431.4:c.2431G= XP_005266488.1:p.Glu811=
XM_006719837.3:c.2371G= XP_006719900.1:p.Glu791=
XM_011535117.3:c.2371G= XP_011533419.1:p.Glu791=
XM_017020627.1:c.2371G= XP_016876116.1:p.Glu791=
NM_000053.4:c.2467G= MANE Select NP_000044.2:p.Glu823=
NM_001005918.3:c.1981G= NP_001005918.1:p.Glu661=
NM_001330579.2:c.2215G= NP_001317508.1:p.Glu739=
NM_001243182.2:c.2134G= NP_001230111.1:p.Glu712=
NM_001330578.2:c.2233G= NP_001317507.1:p.Glu745=