Canonical Allele Identifier: CA2091559557
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51941188T= , CM000675.2:g.51941188T= GRCh38
NC_000013.10:g.52515324T= , CM000675.1:g.52515324T= GRCh37
NC_000013.9:g.51413325T= NCBI36
NG_008806.1:g.75307A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*1099A= ENSP00000489512.2:n.*1099A=
ENST00000673864.2:c.*2193A= ENSP00000501045.2:n.*2193A=
ENST00000674147.2:c.2828A= ENSP00000500964.2:p.Asn943=
ENST00000242839.10:c.3449A= MANE Select ENSP00000242839.5:p.Asn1150=
ENST00000344297.9:c.2828A= ENSP00000342559.5:p.Asn943=
ENST00000400366.6:c.3116A= ENSP00000383217.3:p.Asn1039=
ENST00000448424.7:c.3197A= ENSP00000416738.3:p.Asn1066=
ENST00000673772.1:c.3215A= ENSP00000501168.1:p.Asn1072=
ENST00000673867.1:n.3588A=
ENST00000674126.1:n.3812A=
ENST00000674147.1:c.2384A= ENSP00000500964.1:p.Asn795=
ENST00000242839.8:c.3449A= ENSP00000242839.4:p.Asn1150=
ENST00000344297.8:c.2828A= ENSP00000342559.5:p.Asn943=
ENST00000400366.5:c.3116A= ENSP00000383217.3:p.Asn1039=
ENST00000400370.8:c.2159A= ENSP00000383221.3:p.Asn720=
ENST00000418097.7:c.3254A= ENSP00000393343.2:p.Asn1085=
ENST00000448424.6:c.3215A= ENSP00000416738.2:p.Asn1072=
ENST00000634296.1:c.1227A=
ENST00000634308.1:c.*550A= ENSP00000489234.1:n.*550A=
ENST00000634620.1:n.4193A=
ENST00000634810.1:n.2794A=
ENST00000634844.1:c.3305A= ENSP00000489398.1:p.Asn1102=
NM_000053.3:c.3449A= NP_000044.2:p.Asn1150=
NM_001005918.2:c.2828A= NP_001005918.1:p.Asn943=
NM_001243182.1:c.3116A= NP_001230111.1:p.Asn1039=
XM_005266423.2:c.3353A= XP_005266480.1:p.Asn1118=
XM_005266424.3:c.3353A= XP_005266481.1:p.Asn1118=
XM_005266427.2:c.3215A= XP_005266484.1:p.Asn1072=
XM_005266428.1:c.3197A= XP_005266485.1:p.Asn1066=
XM_005266430.3:c.3449A= XP_005266487.1:p.Asn1150=
XM_005266431.2:c.3413A= XP_005266488.1:p.Asn1138=
XM_005266432.2:c.2963A= XP_005266489.1:p.Asn988=
XM_006719837.2:c.3353A= XP_006719900.1:p.Asn1118=
XM_006719838.1:c.1265A= XP_006719901.1:p.Asn422=
XM_006719839.1:c.1082A= XP_006719902.1:p.Asn361=
XM_011535117.1:c.3353A= XP_011533419.1:p.Asn1118=
XM_011535118.1:c.3314A= XP_011533420.1:p.Asn1105=
XM_011535119.1:c.3266A= XP_011533421.1:p.Asn1089=
XM_011535120.1:c.3035A= XP_011533422.1:p.Asn1012=
XM_011535121.1:c.2936A= XP_011533423.1:p.Asn979=
XM_011535122.1:c.2117A= XP_011533424.1:p.Asn706=
XR_941601.1:n.3668A=
XR_941602.1:n.3668A=
XR_941603.1:n.3668A=
XR_941604.1:n.3668A=
NM_001330578.1:c.3215A= NP_001317507.1:p.Asn1072=
NM_001330579.1:c.3197A= NP_001317508.1:p.Asn1066=
XM_005266424.4:c.3353A= XP_005266481.1:p.Asn1118=
XM_005266430.4:c.3449A= XP_005266487.1:p.Asn1150=
XM_005266431.4:c.3413A= XP_005266488.1:p.Asn1138=
XM_006719837.3:c.3353A= XP_006719900.1:p.Asn1118=
XM_011535117.3:c.3353A= XP_011533419.1:p.Asn1118=
XM_017020627.1:c.3353A= XP_016876116.1:p.Asn1118=
NM_000053.4:c.3449A= MANE Select NP_000044.2:p.Asn1150=
NM_001005918.3:c.2828A= NP_001005918.1:p.Asn943=
NM_001330579.2:c.3197A= NP_001317508.1:p.Asn1066=
NM_001243182.2:c.3116A= NP_001230111.1:p.Asn1039=
NM_001330578.2:c.3215A= NP_001317507.1:p.Asn1072=