Canonical Allele Identifier: CA2091559389
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51941114T= , CM000675.2:g.51941114T= GRCh38
NC_000013.10:g.52515250T= , CM000675.1:g.52515250T= GRCh37
NC_000013.9:g.51413251T= NCBI36
NG_008806.1:g.75381A=

Transcript Alleles

HGVS Amino-acid change
ENST00000634296.2:c.*1173A= ENSP00000489512.2:n.*1173A=
ENST00000673864.2:c.*2267A= ENSP00000501045.2:n.*2267A=
ENST00000674147.2:c.2902A= ENSP00000500964.2:p.Lys968=
ENST00000242839.10:c.3523A= MANE Select ENSP00000242839.5:p.Lys1175=
ENST00000344297.9:c.2902A= ENSP00000342559.5:p.Lys968=
ENST00000400366.6:c.3190A= ENSP00000383217.3:p.Lys1064=
ENST00000448424.7:c.3271A= ENSP00000416738.3:p.Lys1091=
ENST00000673772.1:c.3289A= ENSP00000501168.1:p.Lys1097=
ENST00000673867.1:n.3662A=
ENST00000674126.1:n.3886A=
ENST00000674147.1:c.2458A= ENSP00000500964.1:p.Lys820=
ENST00000242839.8:c.3523A= ENSP00000242839.4:p.Lys1175=
ENST00000344297.8:c.2902A= ENSP00000342559.5:p.Lys968=
ENST00000400366.5:c.3190A= ENSP00000383217.3:p.Lys1064=
ENST00000400370.8:c.2233A= ENSP00000383221.3:p.Lys745=
ENST00000418097.7:c.3328A= ENSP00000393343.2:p.Lys1110=
ENST00000448424.6:c.3289A= ENSP00000416738.2:p.Lys1097=
ENST00000634296.1:c.1301A=
ENST00000634308.1:c.*624A= ENSP00000489234.1:n.*624A=
ENST00000634620.1:n.4267A=
ENST00000634810.1:n.2868A=
ENST00000634844.1:c.3379A= ENSP00000489398.1:p.Lys1127=
NM_000053.3:c.3523A= NP_000044.2:p.Lys1175=
NM_001005918.2:c.2902A= NP_001005918.1:p.Lys968=
NM_001243182.1:c.3190A= NP_001230111.1:p.Lys1064=
XM_005266423.2:c.3427A= XP_005266480.1:p.Lys1143=
XM_005266424.3:c.3427A= XP_005266481.1:p.Lys1143=
XM_005266427.2:c.3289A= XP_005266484.1:p.Lys1097=
XM_005266428.1:c.3271A= XP_005266485.1:p.Lys1091=
XM_005266430.3:c.3523A= XP_005266487.1:p.Lys1175=
XM_005266431.2:c.3487A= XP_005266488.1:p.Lys1163=
XM_005266432.2:c.3037A= XP_005266489.1:p.Lys1013=
XM_006719837.2:c.3427A= XP_006719900.1:p.Lys1143=
XM_006719838.1:c.1339A= XP_006719901.1:p.Lys447=
XM_006719839.1:c.1156A= XP_006719902.1:p.Lys386=
XM_011535117.1:c.3427A= XP_011533419.1:p.Lys1143=
XM_011535118.1:c.3388A= XP_011533420.1:p.Lys1130=
XM_011535119.1:c.3340A= XP_011533421.1:p.Lys1114=
XM_011535120.1:c.3109A= XP_011533422.1:p.Lys1037=
XM_011535121.1:c.3010A= XP_011533423.1:p.Lys1004=
XM_011535122.1:c.2191A= XP_011533424.1:p.Lys731=
XR_941601.1:n.3742A=
XR_941602.1:n.3742A=
XR_941603.1:n.3742A=
XR_941604.1:n.3742A=
NM_001330578.1:c.3289A= NP_001317507.1:p.Lys1097=
NM_001330579.1:c.3271A= NP_001317508.1:p.Lys1091=
XM_005266424.4:c.3427A= XP_005266481.1:p.Lys1143=
XM_005266430.4:c.3523A= XP_005266487.1:p.Lys1175=
XM_005266431.4:c.3487A= XP_005266488.1:p.Lys1163=
XM_006719837.3:c.3427A= XP_006719900.1:p.Lys1143=
XM_011535117.3:c.3427A= XP_011533419.1:p.Lys1143=
XM_017020627.1:c.3427A= XP_016876116.1:p.Lys1143=
NM_000053.4:c.3523A= MANE Select NP_000044.2:p.Lys1175=
NM_001005918.3:c.2902A= NP_001005918.1:p.Lys968=
NM_001330579.2:c.3271A= NP_001317508.1:p.Lys1091=
NM_001243182.2:c.3190A= NP_001230111.1:p.Lys1064=
NM_001330578.2:c.3289A= NP_001317507.1:p.Lys1097=