Canonical Allele Identifier: CA609969207
Gene: ATP7B HGNC NCBI

Linked Data

dbSNP Id: rs895072034

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51960477_51960480del , CM000675.2:g.51960477_51960480del GRCh38
NC_000013.10:g.52534613_52534616del , CM000675.1:g.52534613_52534616del GRCh37
NC_000013.9:g.51432614_51432617del NCBI36
NG_008806.1:g.56023_56026del

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.1946+1365_1946+1368del ENSP00000489512.2:n.1946+1365_1946+1368del
ENST00000673864.2:c.*691-150_*691-147del ENSP00000501045.2:n.*691-150_*691-147del
ENST00000674147.2:c.1870-2865_1870-2862del ENSP00000500964.2:n.1870-2865_1870-2862del
ENST00000242839.10:c.1947-150_1947-147del MANE Select ENSP00000242839.5:n.1947-150_1947-147del
ENST00000344297.9:c.1870-2865_1870-2862del ENSP00000342559.5:n.1870-2865_1870-2862del
ENST00000400366.6:c.1614-150_1614-147del ENSP00000383217.3:n.1614-150_1614-147del
ENST00000448424.7:c.1870-1928_1870-1925del ENSP00000416738.3:n.1870-1928_1870-1925del
ENST00000673772.1:c.1947-150_1947-147del ENSP00000501168.1:n.1947-150_1947-147del
ENST00000674147.1:c.1426-2865_1426-2862del ENSP00000500964.1:n.1426-2865_1426-2862del
ENST00000242839.8:c.1947-150_1947-147del ENSP00000242839.4:n.1947-150_1947-147del
ENST00000344297.8:c.1870-2865_1870-2862del ENSP00000342559.5:n.1870-2865_1870-2862del
ENST00000400366.5:c.1614-150_1614-147del ENSP00000383217.3:n.1614-150_1614-147del
ENST00000400370.8:c.1286-10311_1286-10308del ENSP00000383221.3:n.1286-10311_1286-10308del
ENST00000418097.7:c.1947-150_1947-147del ENSP00000393343.2:n.1947-150_1947-147del
ENST00000448424.6:c.1947-150_1947-147del ENSP00000416738.2:n.1947-150_1947-147del
ENST00000482841.6:n.1665-1928_1665-1925del
ENST00000634296.1:c.82+1365_82+1368del
ENST00000634308.1:c.1947-150_1947-147del ENSP00000489234.1:n.1947-150_1947-147del
ENST00000634620.1:n.439-150_439-147del
ENST00000634844.1:c.1947-150_1947-147del ENSP00000489398.1:n.1947-150_1947-147del
ENST00000635406.1:n.212-13994_212-13991del
NM_000053.3:c.1947-150_1947-147del NP_000044.2:n.1947-150_1947-147del
NM_001005918.2:c.1870-2865_1870-2862del NP_001005918.1:n.1870-2865_1870-2862del
NM_001243182.1:c.1614-150_1614-147del NP_001230111.1:n.1614-150_1614-147del
XM_005266423.2:c.1851-150_1851-147del XP_005266480.1:n.1851-150_1851-147del
XM_005266424.3:c.1851-150_1851-147del XP_005266481.1:n.1851-150_1851-147del
XM_005266427.2:c.1947-150_1947-147del XP_005266484.1:n.1947-150_1947-147del
XM_005266428.1:c.1870-1928_1870-1925del XP_005266485.1:n.1870-1928_1870-1925del
XM_005266430.3:c.1947-150_1947-147del XP_005266487.1:n.1947-150_1947-147del
XM_005266431.2:c.1911-150_1911-147del XP_005266488.1:n.1911-150_1911-147del
XM_005266432.2:c.1870-2865_1870-2862del XP_005266489.1:n.1870-2865_1870-2862del
XM_006719837.2:c.1851-150_1851-147del XP_006719900.1:n.1851-150_1851-147del
XM_006719838.1:c.-64+1365_-64+1368del XP_006719901.1:n.-64+1365_-64+1368del
XM_006719839.1:c.-64+1365_-64+1368del XP_006719902.1:n.-64+1365_-64+1368del
XM_011535117.1:c.1851-150_1851-147del XP_011533419.1:n.1851-150_1851-147del
XM_011535118.1:c.1947-150_1947-147del XP_011533420.1:n.1947-150_1947-147del
XM_011535119.1:c.1947-150_1947-147del XP_011533421.1:n.1947-150_1947-147del
XM_011535120.1:c.1708-1928_1708-1925del XP_011533422.1:n.1708-1928_1708-1925del
XM_011535121.1:c.1947-150_1947-147del XP_011533423.1:n.1947-150_1947-147del
XM_011535122.1:c.615-150_615-147del XP_011533424.1:n.615-150_615-147del
XR_941601.1:n.2166-150_2166-147del
XR_941602.1:n.2166-150_2166-147del
XR_941603.1:n.2166-150_2166-147del
XR_941604.1:n.2166-150_2166-147del
NM_001330578.1:c.1947-150_1947-147del NP_001317507.1:n.1947-150_1947-147del
NM_001330579.1:c.1870-1928_1870-1925del NP_001317508.1:n.1870-1928_1870-1925del
XM_005266424.4:c.1851-150_1851-147del XP_005266481.1:n.1851-150_1851-147del
XM_005266430.4:c.1947-150_1947-147del XP_005266487.1:n.1947-150_1947-147del
XM_005266431.4:c.1911-150_1911-147del XP_005266488.1:n.1911-150_1911-147del
XM_006719837.3:c.1851-150_1851-147del XP_006719900.1:n.1851-150_1851-147del
XM_011535117.3:c.1851-150_1851-147del XP_011533419.1:n.1851-150_1851-147del
XM_017020627.1:c.1851-150_1851-147del XP_016876116.1:n.1851-150_1851-147del
NM_000053.4:c.1947-150_1947-147del MANE Select NP_000044.2:n.1947-150_1947-147del
NM_001005918.3:c.1870-2865_1870-2862del NP_001005918.1:n.1870-2865_1870-2862del
NM_001330579.2:c.1870-1928_1870-1925del NP_001317508.1:n.1870-1928_1870-1925del
NM_001243182.2:c.1614-150_1614-147del NP_001230111.1:n.1614-150_1614-147del
NM_001330578.2:c.1947-150_1947-147del NP_001317507.1:n.1947-150_1947-147del