Canonical Allele Identifier: CA2018046968
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51941218A= , CM000675.2:g.51941218A= GRCh38
NC_000013.10:g.52515354A= , CM000675.1:g.52515354A= GRCh37
NC_000013.9:g.51413355A= NCBI36
NG_008806.1:g.75277T=

Transcript Alleles

HGVS Amino-acid change
ENST00000634296.2:c.*1069T= ENSP00000489512.2:n.*1069T=
ENST00000673864.2:c.*2163T= ENSP00000501045.2:n.*2163T=
ENST00000674147.2:c.2798T= ENSP00000500964.2:p.Val933=
ENST00000242839.10:c.3419T= MANE Select ENSP00000242839.5:p.Val1140=
ENST00000344297.9:c.2798T= ENSP00000342559.5:p.Val933=
ENST00000400366.6:c.3086T= ENSP00000383217.3:p.Val1029=
ENST00000448424.7:c.3167T= ENSP00000416738.3:p.Val1056=
ENST00000673772.1:c.3185T= ENSP00000501168.1:p.Val1062=
ENST00000673867.1:n.3558T=
ENST00000674126.1:n.3782T=
ENST00000674147.1:c.2354T= ENSP00000500964.1:p.Val785=
ENST00000242839.8:c.3419T= ENSP00000242839.4:p.Val1140=
ENST00000344297.8:c.2798T= ENSP00000342559.5:p.Val933=
ENST00000400366.5:c.3086T= ENSP00000383217.3:p.Val1029=
ENST00000400370.8:c.2129T= ENSP00000383221.3:p.Val710=
ENST00000418097.7:c.3224T= ENSP00000393343.2:p.Val1075=
ENST00000448424.6:c.3185T= ENSP00000416738.2:p.Val1062=
ENST00000634296.1:c.1197T=
ENST00000634308.1:c.*520T= ENSP00000489234.1:n.*520T=
ENST00000634620.1:n.4163T=
ENST00000634810.1:n.2764T=
ENST00000634844.1:c.3275T= ENSP00000489398.1:p.Val1092=
NM_000053.3:c.3419T= NP_000044.2:p.Val1140=
NM_001005918.2:c.2798T= NP_001005918.1:p.Val933=
NM_001243182.1:c.3086T= NP_001230111.1:p.Val1029=
XM_005266423.2:c.3323T= XP_005266480.1:p.Val1108=
XM_005266424.3:c.3323T= XP_005266481.1:p.Val1108=
XM_005266427.2:c.3185T= XP_005266484.1:p.Val1062=
XM_005266428.1:c.3167T= XP_005266485.1:p.Val1056=
XM_005266430.3:c.3419T= XP_005266487.1:p.Val1140=
XM_005266431.2:c.3383T= XP_005266488.1:p.Val1128=
XM_005266432.2:c.2933T= XP_005266489.1:p.Val978=
XM_006719837.2:c.3323T= XP_006719900.1:p.Val1108=
XM_006719838.1:c.1235T= XP_006719901.1:p.Val412=
XM_006719839.1:c.1052T= XP_006719902.1:p.Val351=
XM_011535117.1:c.3323T= XP_011533419.1:p.Val1108=
XM_011535118.1:c.3284T= XP_011533420.1:p.Val1095=
XM_011535119.1:c.3236T= XP_011533421.1:p.Val1079=
XM_011535120.1:c.3005T= XP_011533422.1:p.Val1002=
XM_011535121.1:c.2906T= XP_011533423.1:p.Val969=
XM_011535122.1:c.2087T= XP_011533424.1:p.Val696=
XR_941601.1:n.3638T=
XR_941602.1:n.3638T=
XR_941603.1:n.3638T=
XR_941604.1:n.3638T=
NM_001330578.1:c.3185T= NP_001317507.1:p.Val1062=
NM_001330579.1:c.3167T= NP_001317508.1:p.Val1056=
XM_005266424.4:c.3323T= XP_005266481.1:p.Val1108=
XM_005266430.4:c.3419T= XP_005266487.1:p.Val1140=
XM_005266431.4:c.3383T= XP_005266488.1:p.Val1128=
XM_006719837.3:c.3323T= XP_006719900.1:p.Val1108=
XM_011535117.3:c.3323T= XP_011533419.1:p.Val1108=
XM_017020627.1:c.3323T= XP_016876116.1:p.Val1108=
NM_000053.4:c.3419T= MANE Select NP_000044.2:p.Val1140=
NM_001005918.3:c.2798T= NP_001005918.1:p.Val933=
NM_001330579.2:c.3167T= NP_001317508.1:p.Val1056=
NM_001243182.2:c.3086T= NP_001230111.1:p.Val1029=
NM_001330578.2:c.3185T= NP_001317507.1:p.Val1062=