Canonical Allele Identifier: CA2091541941
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2679837
ClinVar RCV Id: RCV003474242
dbSNP Id: rs1957900892

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51950078del , CM000675.2:g.51950078del GRCh38
NC_000013.10:g.52524214del , CM000675.1:g.52524214del GRCh37
NC_000013.9:g.51422215del NCBI36
NG_008806.1:g.66417del

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*492del ENSP00000489512.2:n.*492del
ENST00000673864.2:c.*1403del ENSP00000501045.2:n.*1403del
ENST00000674147.2:c.2173del ENSP00000500964.2:p.Ala725LeufsTer14
ENST00000242839.10:c.2659del MANE Select ENSP00000242839.5:p.Ala887LeufsTer14
ENST00000344297.9:c.2173del ENSP00000342559.5:p.Ala725LeufsTer14
ENST00000400366.6:c.2326del ENSP00000383217.3:p.Ala776LeufsTer14
ENST00000448424.7:c.2407del ENSP00000416738.3:p.Ala803LeufsTer14
ENST00000673772.1:c.2425del ENSP00000501168.1:p.Ala809LeufsTer14
ENST00000674147.1:c.1729del ENSP00000500964.1:p.Ala577LeufsTer14
ENST00000242839.8:c.2659del ENSP00000242839.4:p.Ala887LeufsTer14
ENST00000344297.8:c.2173del ENSP00000342559.5:p.Ala725LeufsTer14
ENST00000400366.5:c.2326del ENSP00000383217.3:p.Ala776LeufsTer14
ENST00000400370.8:c.1369del ENSP00000383221.3:p.Ala457LeufsTer14
ENST00000418097.7:c.2659del ENSP00000393343.2:p.Ala887LeufsTer14
ENST00000448424.6:c.2425del ENSP00000416738.2:p.Ala809LeufsTer14
ENST00000634296.1:c.620del
ENST00000634308.1:c.2425del ENSP00000489234.1:p.Ala809LeufsTer14
ENST00000634620.1:n.3457del
ENST00000634810.1:n.2004del
ENST00000634844.1:c.2515del ENSP00000489398.1:p.Ala839LeufsTer14
ENST00000635406.1:n.212-3600del
NM_000053.3:c.2659del NP_000044.2:p.Ala887LeufsTer14
NM_001005918.2:c.2173del NP_001005918.1:p.Ala725LeufsTer14
NM_001243182.1:c.2326del NP_001230111.1:p.Ala776LeufsTer14
XM_005266423.2:c.2563del XP_005266480.1:p.Ala855LeufsTer14
XM_005266424.3:c.2563del XP_005266481.1:p.Ala855LeufsTer14
XM_005266427.2:c.2425del XP_005266484.1:p.Ala809LeufsTer14
XM_005266428.1:c.2407del XP_005266485.1:p.Ala803LeufsTer14
XM_005266430.3:c.2659del XP_005266487.1:p.Ala887LeufsTer14
XM_005266431.2:c.2623del XP_005266488.1:p.Ala875LeufsTer14
XM_005266432.2:c.2173del XP_005266489.1:p.Ala725LeufsTer14
XM_006719837.2:c.2563del XP_006719900.1:p.Ala855LeufsTer14
XM_006719838.1:c.475del XP_006719901.1:p.Ala159LeufsTer14
XM_006719839.1:c.475del XP_006719902.1:p.Ala159LeufsTer14
XM_011535117.1:c.2563del XP_011533419.1:p.Ala855LeufsTer14
XM_011535118.1:c.2659del XP_011533420.1:p.Ala887LeufsTer14
XM_011535119.1:c.2659del XP_011533421.1:p.Ala887LeufsTer14
XM_011535120.1:c.2245del XP_011533422.1:p.Ala749LeufsTer14
XM_011535121.1:c.2659del XP_011533423.1:p.Ala887LeufsTer14
XM_011535122.1:c.1327del XP_011533424.1:p.Ala443LeufsTer14
XR_941601.1:n.2878del
XR_941602.1:n.2878del
XR_941603.1:n.2878del
XR_941604.1:n.2878del
NM_001330578.1:c.2425del NP_001317507.1:p.Ala809LeufsTer14
NM_001330579.1:c.2407del NP_001317508.1:p.Ala803LeufsTer14
XM_005266424.4:c.2563del XP_005266481.1:p.Ala855LeufsTer14
XM_005266430.4:c.2659del XP_005266487.1:p.Ala887LeufsTer14
XM_005266431.4:c.2623del XP_005266488.1:p.Ala875LeufsTer14
XM_006719837.3:c.2563del XP_006719900.1:p.Ala855LeufsTer14
XM_011535117.3:c.2563del XP_011533419.1:p.Ala855LeufsTer14
XM_017020627.1:c.2563del XP_016876116.1:p.Ala855LeufsTer14
NM_000053.4:c.2659del MANE Select NP_000044.2:p.Ala887LeufsTer14
NM_001005918.3:c.2173del NP_001005918.1:p.Ala725LeufsTer14
NM_001330579.2:c.2407del NP_001317508.1:p.Ala803LeufsTer14
NM_001243182.2:c.2326del NP_001230111.1:p.Ala776LeufsTer14
NM_001330578.2:c.2425del NP_001317507.1:p.Ala809LeufsTer14