Canonical Allele Identifier: CA2091541360
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51949708A= , CM000675.2:g.51949708A= GRCh38
NC_000013.10:g.52523844A= , CM000675.1:g.52523844A= GRCh37
NC_000013.9:g.51421845A= NCBI36
NG_008806.1:g.66787T=

Transcript Alleles

HGVS Amino-acid change
ENST00000634296.2:c.*652T= ENSP00000489512.2:n.*652T=
ENST00000673864.2:c.*1563T= ENSP00000501045.2:n.*1563T=
ENST00000674147.2:c.2244+299T= ENSP00000500964.2:n.2244+299T=
ENST00000242839.10:c.2819T= MANE Select ENSP00000242839.5:p.Ile940=
ENST00000344297.9:c.2244+299T= ENSP00000342559.5:n.2244+299T=
ENST00000400366.6:c.2486T= ENSP00000383217.3:p.Ile829=
ENST00000448424.7:c.2567T= ENSP00000416738.3:p.Ile856=
ENST00000673772.1:c.2585T= ENSP00000501168.1:p.Ile862=
ENST00000674147.1:c.1800+299T= ENSP00000500964.1:n.1800+299T=
ENST00000242839.8:c.2819T= ENSP00000242839.4:p.Ile940=
ENST00000344297.8:c.2244+299T= ENSP00000342559.5:n.2244+299T=
ENST00000400366.5:c.2486T= ENSP00000383217.3:p.Ile829=
ENST00000400370.8:c.1529T= ENSP00000383221.3:p.Ile510=
ENST00000418097.7:c.2819T= ENSP00000393343.2:p.Ile940=
ENST00000448424.6:c.2585T= ENSP00000416738.2:p.Ile862=
ENST00000634296.1:c.780T=
ENST00000634308.1:c.2585T= ENSP00000489234.1:p.Ile862=
ENST00000634620.1:n.3609+8T=
ENST00000634810.1:n.2164T=
ENST00000634844.1:c.2675T= ENSP00000489398.1:p.Ile892=
ENST00000635406.1:n.212-3230T=
NM_000053.3:c.2819T= NP_000044.2:p.Ile940=
NM_001005918.2:c.2244+299T= NP_001005918.1:n.2244+299T=
NM_001243182.1:c.2486T= NP_001230111.1:p.Ile829=
XM_005266423.2:c.2723T= XP_005266480.1:p.Ile908=
XM_005266424.3:c.2723T= XP_005266481.1:p.Ile908=
XM_005266427.2:c.2585T= XP_005266484.1:p.Ile862=
XM_005266428.1:c.2567T= XP_005266485.1:p.Ile856=
XM_005266430.3:c.2819T= XP_005266487.1:p.Ile940=
XM_005266431.2:c.2783T= XP_005266488.1:p.Ile928=
XM_005266432.2:c.2333T= XP_005266489.1:p.Ile778=
XM_006719837.2:c.2723T= XP_006719900.1:p.Ile908=
XM_006719838.1:c.635T= XP_006719901.1:p.Ile212=
XM_006719839.1:c.635T= XP_006719902.1:p.Ile212=
XM_011535117.1:c.2723T= XP_011533419.1:p.Ile908=
XM_011535118.1:c.2730+299T= XP_011533420.1:n.2730+299T=
XM_011535119.1:c.2819T= XP_011533421.1:p.Ile940=
XM_011535120.1:c.2405T= XP_011533422.1:p.Ile802=
XM_011535121.1:c.2730+299T= XP_011533423.1:n.2730+299T=
XM_011535122.1:c.1487T= XP_011533424.1:p.Ile496=
XR_941601.1:n.3038T=
XR_941602.1:n.3038T=
XR_941603.1:n.3038T=
XR_941604.1:n.3038T=
NM_001330578.1:c.2585T= NP_001317507.1:p.Ile862=
NM_001330579.1:c.2567T= NP_001317508.1:p.Ile856=
XM_005266424.4:c.2723T= XP_005266481.1:p.Ile908=
XM_005266430.4:c.2819T= XP_005266487.1:p.Ile940=
XM_005266431.4:c.2783T= XP_005266488.1:p.Ile928=
XM_006719837.3:c.2723T= XP_006719900.1:p.Ile908=
XM_011535117.3:c.2723T= XP_011533419.1:p.Ile908=
XM_017020627.1:c.2723T= XP_016876116.1:p.Ile908=
NM_000053.4:c.2819T= MANE Select NP_000044.2:p.Ile940=
NM_001005918.3:c.2244+299T= NP_001005918.1:n.2244+299T=
NM_001330579.2:c.2567T= NP_001317508.1:p.Ile856=
NM_001243182.2:c.2486T= NP_001230111.1:p.Ile829=
NM_001330578.2:c.2585T= NP_001317507.1:p.Ile862=