Canonical Allele Identifier: CA2623117085
Gene: ATP7B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51946260G>C , CM000675.2:g.51946260G>C GRCh38
NC_000013.10:g.52520396G>C , CM000675.1:g.52520396G>C GRCh37
NC_000013.9:g.51418397G>C NCBI36
NG_008806.1:g.70235C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*893+24C>G ENSP00000489512.2:n.*893+24C>G
ENST00000673864.2:c.*1804+24C>G ENSP00000501045.2:n.*1804+24C>G
ENST00000674147.2:c.2439+24C>G ENSP00000500964.2:n.2439+24C>G
ENST00000242839.10:c.3060+24C>G MANE Select ENSP00000242839.5:n.3060+24C>G
ENST00000344297.9:c.2439+24C>G ENSP00000342559.5:n.2439+24C>G
ENST00000400366.6:c.2727+24C>G ENSP00000383217.3:n.2727+24C>G
ENST00000448424.7:c.2808+24C>G ENSP00000416738.3:n.2808+24C>G
ENST00000673772.1:c.2826+24C>G ENSP00000501168.1:n.2826+24C>G
ENST00000673867.1:n.1231C>G
ENST00000674126.1:n.3423+24C>G
ENST00000674147.1:c.1995+24C>G ENSP00000500964.1:n.1995+24C>G
ENST00000242839.8:c.3060+24C>G ENSP00000242839.4:n.3060+24C>G
ENST00000344297.8:c.2439+24C>G ENSP00000342559.5:n.2439+24C>G
ENST00000400366.5:c.2727+24C>G ENSP00000383217.3:n.2727+24C>G
ENST00000400370.8:c.1770+24C>G ENSP00000383221.3:n.1770+24C>G
ENST00000418097.7:c.2866-1969C>G ENSP00000393343.2:n.2866-1969C>G
ENST00000448424.6:c.2826+24C>G ENSP00000416738.2:n.2826+24C>G
ENST00000466629.1:n.280+24C>G
ENST00000634296.1:c.1021+24C>G
ENST00000634308.1:c.*161+24C>G ENSP00000489234.1:n.*161+24C>G
ENST00000634620.1:n.3804+24C>G
ENST00000634810.1:n.2405+24C>G
ENST00000634844.1:c.2916+24C>G ENSP00000489398.1:n.2916+24C>G
ENST00000635406.1:n.406+24C>G
NM_000053.3:c.3060+24C>G NP_000044.2:n.3060+24C>G
NM_001005918.2:c.2439+24C>G NP_001005918.1:n.2439+24C>G
NM_001243182.1:c.2727+24C>G NP_001230111.1:n.2727+24C>G
XM_005266423.2:c.2964+24C>G XP_005266480.1:n.2964+24C>G
XM_005266424.3:c.2964+24C>G XP_005266481.1:n.2964+24C>G
XM_005266427.2:c.2826+24C>G XP_005266484.1:n.2826+24C>G
XM_005266428.1:c.2808+24C>G XP_005266485.1:n.2808+24C>G
XM_005266430.3:c.3060+24C>G XP_005266487.1:n.3060+24C>G
XM_005266431.2:c.3024+24C>G XP_005266488.1:n.3024+24C>G
XM_005266432.2:c.2574+24C>G XP_005266489.1:n.2574+24C>G
XM_006719837.2:c.2964+24C>G XP_006719900.1:n.2964+24C>G
XM_006719838.1:c.876+24C>G XP_006719901.1:n.876+24C>G
XM_006719839.1:c.876+24C>G XP_006719902.1:n.876+24C>G
XM_011535117.1:c.2964+24C>G XP_011533419.1:n.2964+24C>G
XM_011535118.1:c.2925+24C>G XP_011533420.1:n.2925+24C>G
XM_011535119.1:c.3060+24C>G XP_011533421.1:n.3060+24C>G
XM_011535120.1:c.2646+24C>G XP_011533422.1:n.2646+24C>G
XM_011535121.1:c.2731-3706C>G XP_011533423.1:n.2731-3706C>G
XM_011535122.1:c.1728+24C>G XP_011533424.1:n.1728+24C>G
XR_941601.1:n.3279+24C>G
XR_941602.1:n.3279+24C>G
XR_941603.1:n.3279+24C>G
XR_941604.1:n.3279+24C>G
NM_001330578.1:c.2826+24C>G NP_001317507.1:n.2826+24C>G
NM_001330579.1:c.2808+24C>G NP_001317508.1:n.2808+24C>G
XM_005266424.4:c.2964+24C>G XP_005266481.1:n.2964+24C>G
XM_005266430.4:c.3060+24C>G XP_005266487.1:n.3060+24C>G
XM_005266431.4:c.3024+24C>G XP_005266488.1:n.3024+24C>G
XM_006719837.3:c.2964+24C>G XP_006719900.1:n.2964+24C>G
XM_011535117.3:c.2964+24C>G XP_011533419.1:n.2964+24C>G
XM_017020627.1:c.2964+24C>G XP_016876116.1:n.2964+24C>G
NM_000053.4:c.3060+24C>G MANE Select NP_000044.2:n.3060+24C>G
NM_001005918.3:c.2439+24C>G NP_001005918.1:n.2439+24C>G
NM_001330579.2:c.2808+24C>G NP_001317508.1:n.2808+24C>G
NM_001243182.2:c.2727+24C>G NP_001230111.1:n.2727+24C>G
NM_001330578.2:c.2826+24C>G NP_001317507.1:n.2826+24C>G