Canonical Allele Identifier: CA2536168370
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51946531del , CM000675.2:g.51946531del GRCh38
NC_000013.10:g.52520667del , CM000675.1:g.52520667del GRCh37
NC_000013.9:g.51418668del NCBI36
NG_008806.1:g.69966del

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*699-51del ENSP00000489512.2:n.*699-51del
ENST00000673864.2:c.*1610-51del ENSP00000501045.2:n.*1610-51del
ENST00000674147.2:c.2245-51del ENSP00000500964.2:n.2245-51del
ENST00000242839.10:c.2866-51del MANE Select ENSP00000242839.5:n.2866-51del
ENST00000344297.9:c.2245-51del ENSP00000342559.5:n.2245-51del
ENST00000400366.6:c.2533-51del ENSP00000383217.3:n.2533-51del
ENST00000448424.7:c.2614-51del ENSP00000416738.3:n.2614-51del
ENST00000673772.1:c.2632-51del ENSP00000501168.1:n.2632-51del
ENST00000673867.1:n.962del
ENST00000674126.1:n.3178del
ENST00000674147.1:c.1801-51del ENSP00000500964.1:n.1801-51del
ENST00000242839.8:c.2866-51del ENSP00000242839.4:n.2866-51del
ENST00000344297.8:c.2245-51del ENSP00000342559.5:n.2245-51del
ENST00000400366.5:c.2533-51del ENSP00000383217.3:n.2533-51del
ENST00000400370.8:c.1576-51del ENSP00000383221.3:n.1576-51del
ENST00000418097.7:c.2866-2238del ENSP00000393343.2:n.2866-2238del
ENST00000448424.6:c.2632-51del ENSP00000416738.2:n.2632-51del
ENST00000466629.1:n.35del
ENST00000634296.1:c.827-51del
ENST00000634308.1:c.2652-51del ENSP00000489234.1:n.2652-51del
ENST00000634620.1:n.3610-51del
ENST00000634810.1:n.2211-51del
ENST00000634844.1:c.2722-51del ENSP00000489398.1:n.2722-51del
ENST00000635406.1:n.212-51del
NM_000053.3:c.2866-51del NP_000044.2:n.2866-51del
NM_001005918.2:c.2245-51del NP_001005918.1:n.2245-51del
NM_001243182.1:c.2533-51del NP_001230111.1:n.2533-51del
XM_005266423.2:c.2770-51del XP_005266480.1:n.2770-51del
XM_005266424.3:c.2770-51del XP_005266481.1:n.2770-51del
XM_005266427.2:c.2632-51del XP_005266484.1:n.2632-51del
XM_005266428.1:c.2614-51del XP_005266485.1:n.2614-51del
XM_005266430.3:c.2866-51del XP_005266487.1:n.2866-51del
XM_005266431.2:c.2830-51del XP_005266488.1:n.2830-51del
XM_005266432.2:c.2380-51del XP_005266489.1:n.2380-51del
XM_006719837.2:c.2770-51del XP_006719900.1:n.2770-51del
XM_006719838.1:c.682-51del XP_006719901.1:n.682-51del
XM_006719839.1:c.682-51del XP_006719902.1:n.682-51del
XM_011535117.1:c.2770-51del XP_011533419.1:n.2770-51del
XM_011535118.1:c.2731-51del XP_011533420.1:n.2731-51del
XM_011535119.1:c.2866-51del XP_011533421.1:n.2866-51del
XM_011535120.1:c.2452-51del XP_011533422.1:n.2452-51del
XM_011535121.1:c.2730+3478del XP_011533423.1:n.2730+3478del
XM_011535122.1:c.1534-51del XP_011533424.1:n.1534-51del
XR_941601.1:n.3085-51del
XR_941602.1:n.3085-51del
XR_941603.1:n.3085-51del
XR_941604.1:n.3085-51del
NM_001330578.1:c.2632-51del NP_001317507.1:n.2632-51del
NM_001330579.1:c.2614-51del NP_001317508.1:n.2614-51del
XM_005266424.4:c.2770-51del XP_005266481.1:n.2770-51del
XM_005266430.4:c.2866-51del XP_005266487.1:n.2866-51del
XM_005266431.4:c.2830-51del XP_005266488.1:n.2830-51del
XM_006719837.3:c.2770-51del XP_006719900.1:n.2770-51del
XM_011535117.3:c.2770-51del XP_011533419.1:n.2770-51del
XM_017020627.1:c.2770-51del XP_016876116.1:n.2770-51del
NM_000053.4:c.2866-51del MANE Select NP_000044.2:n.2866-51del
NM_001005918.3:c.2245-51del NP_001005918.1:n.2245-51del
NM_001330579.2:c.2614-51del NP_001317508.1:n.2614-51del
NM_001243182.2:c.2533-51del NP_001230111.1:n.2533-51del
NM_001330578.2:c.2632-51del NP_001317507.1:n.2632-51del