Canonical Allele Identifier: CA2091559571
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51941197A= , CM000675.2:g.51941197A= GRCh38
NC_000013.10:g.52515333A= , CM000675.1:g.52515333A= GRCh37
NC_000013.9:g.51413334A= NCBI36
NG_008806.1:g.75298T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1090T= ENSP00000489512.2:n.*1090T=
ENST00000673864.2:c.*2184T= ENSP00000501045.2:n.*2184T=
ENST00000674147.2:c.2819T= ENSP00000500964.2:p.Leu940=
ENST00000242839.10:c.3440T= MANE Select ENSP00000242839.5:p.Leu1147=
ENST00000344297.9:c.2819T= ENSP00000342559.5:p.Leu940=
ENST00000400366.6:c.3107T= ENSP00000383217.3:p.Leu1036=
ENST00000448424.7:c.3188T= ENSP00000416738.3:p.Leu1063=
ENST00000673772.1:c.3206T= ENSP00000501168.1:p.Leu1069=
ENST00000673867.1:n.3579T=
ENST00000674126.1:n.3803T=
ENST00000674147.1:c.2375T= ENSP00000500964.1:p.Leu792=
ENST00000242839.8:c.3440T= ENSP00000242839.4:p.Leu1147=
ENST00000344297.8:c.2819T= ENSP00000342559.5:p.Leu940=
ENST00000400366.5:c.3107T= ENSP00000383217.3:p.Leu1036=
ENST00000400370.8:c.2150T= ENSP00000383221.3:p.Leu717=
ENST00000418097.7:c.3245T= ENSP00000393343.2:p.Leu1082=
ENST00000448424.6:c.3206T= ENSP00000416738.2:p.Leu1069=
ENST00000634296.1:c.1218T=
ENST00000634308.1:c.*541T= ENSP00000489234.1:n.*541T=
ENST00000634620.1:n.4184T=
ENST00000634810.1:n.2785T=
ENST00000634844.1:c.3296T= ENSP00000489398.1:p.Leu1099=
NM_000053.3:c.3440T= NP_000044.2:p.Leu1147=
NM_001005918.2:c.2819T= NP_001005918.1:p.Leu940=
NM_001243182.1:c.3107T= NP_001230111.1:p.Leu1036=
XM_005266423.2:c.3344T= XP_005266480.1:p.Leu1115=
XM_005266424.3:c.3344T= XP_005266481.1:p.Leu1115=
XM_005266427.2:c.3206T= XP_005266484.1:p.Leu1069=
XM_005266428.1:c.3188T= XP_005266485.1:p.Leu1063=
XM_005266430.3:c.3440T= XP_005266487.1:p.Leu1147=
XM_005266431.2:c.3404T= XP_005266488.1:p.Leu1135=
XM_005266432.2:c.2954T= XP_005266489.1:p.Leu985=
XM_006719837.2:c.3344T= XP_006719900.1:p.Leu1115=
XM_006719838.1:c.1256T= XP_006719901.1:p.Leu419=
XM_006719839.1:c.1073T= XP_006719902.1:p.Leu358=
XM_011535117.1:c.3344T= XP_011533419.1:p.Leu1115=
XM_011535118.1:c.3305T= XP_011533420.1:p.Leu1102=
XM_011535119.1:c.3257T= XP_011533421.1:p.Leu1086=
XM_011535120.1:c.3026T= XP_011533422.1:p.Leu1009=
XM_011535121.1:c.2927T= XP_011533423.1:p.Leu976=
XM_011535122.1:c.2108T= XP_011533424.1:p.Leu703=
XR_941601.1:n.3659T=
XR_941602.1:n.3659T=
XR_941603.1:n.3659T=
XR_941604.1:n.3659T=
NM_001330578.1:c.3206T= NP_001317507.1:p.Leu1069=
NM_001330579.1:c.3188T= NP_001317508.1:p.Leu1063=
XM_005266424.4:c.3344T= XP_005266481.1:p.Leu1115=
XM_005266430.4:c.3440T= XP_005266487.1:p.Leu1147=
XM_005266431.4:c.3404T= XP_005266488.1:p.Leu1135=
XM_006719837.3:c.3344T= XP_006719900.1:p.Leu1115=
XM_011535117.3:c.3344T= XP_011533419.1:p.Leu1115=
XM_017020627.1:c.3344T= XP_016876116.1:p.Leu1115=
NM_000053.4:c.3440T= MANE Select NP_000044.2:p.Leu1147=
NM_001005918.3:c.2819T= NP_001005918.1:p.Leu940=
NM_001330579.2:c.3188T= NP_001317508.1:p.Leu1063=
NM_001243182.2:c.3107T= NP_001230111.1:p.Leu1036=
NM_001330578.2:c.3206T= NP_001317507.1:p.Leu1069=