Canonical Allele Identifier: CA2646571870
Gene: GLMN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92266476_92266479del , CM000663.2:g.92266476_92266479del GRCh38
NC_000001.10:g.92732033_92732036del , CM000663.1:g.92732033_92732036del GRCh37
NC_000001.9:g.92504621_92504624del NCBI36
NG_009796.1:g.37533_37536del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370360.8:c.1156_1159del MANE Select ENSP00000359385.3:p.Ala386CysfsTer22
ENST00000370360.7:c.1156_1159del ENSP00000359385.3:p.Ala386CysfsTer22
ENST00000463560.1:c.562+63_562+66del
ENST00000495106.5:c.1156_1159del ENSP00000436829.1:p.Ala386CysfsTer22
ENST00000495852.6:c.379_382del ENSP00000469157.2:p.Ala127CysfsTer22
NM_053274.2:c.1156_1159del NP_444504.1:p.Ala386CysfsTer22
XM_005270400.1:c.1114_1117del XP_005270457.1:p.Ala372CysfsTer22
XM_005270401.2:c.1030_1033del XP_005270458.1:p.Ala344CysfsTer22
XM_006710309.1:c.655_658del XP_006710372.1:p.Ala219CysfsTer22
XM_011540544.1:c.1156_1159del XP_011538846.1:p.Ala386CysfsTer22
XM_011540545.1:c.1156_1159del XP_011538847.1:p.Ala386CysfsTer22
XM_011540546.1:c.1156_1159del XP_011538848.1:p.Ala386CysfsTer22
XR_946529.1:n.1309+63_1309+66del
NM_001319683.1:c.1114_1117del NP_001306612.1:p.Ala372CysfsTer22
NR_135089.1:n.1271_1274del
XM_005270401.3:c.1030_1033del XP_005270458.1:p.Ala344CysfsTer22
XM_006710309.2:c.655_658del XP_006710372.1:p.Ala219CysfsTer22
XM_011540546.2:c.1156_1159del XP_011538848.1:p.Ala386CysfsTer22
XM_017000137.1:c.1255_1258del XP_016855626.1:p.Ala419CysfsTer22
XM_017000138.1:c.1213_1216del XP_016855627.1:p.Ala405CysfsTer22
XM_017000139.1:c.1293+63_1293+66del XP_016855628.1:n.1293+63_1293+66del
XM_017000140.1:c.1129_1132del XP_016855629.1:p.Ala377CysfsTer22
XM_017000141.1:c.1194+63_1194+66del XP_016855630.1:n.1194+63_1194+66del
XM_017000142.1:c.613_616del XP_016855631.1:p.Ala205CysfsTer22
XM_017000143.1:c.613_616del XP_016855632.1:p.Ala205CysfsTer22
XM_017000144.1:c.385_388del XP_016855633.1:p.Ala129CysfsTer22
XR_002959248.1:n.1677+63_1677+66del
XR_002959249.1:n.1309+63_1309+66del
NM_053274.3:c.1156_1159del MANE Select NP_444504.1:p.Ala386CysfsTer22
NM_001319683.2:c.1114_1117del NP_001306612.1:p.Ala372CysfsTer22
NR_135089.2:n.1249_1252del