Canonical Allele Identifier: CA070786
Gene: GLMN HGNC NCBI

Linked Data

ClinVar Variation Id: 7806
dbSNP Id: rs762515373

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92297411_92297415del , CM000663.2:g.92297411_92297415del GRCh38
NC_000001.10:g.92762968_92762972del , CM000663.1:g.92762968_92762972del GRCh37
NC_000001.9:g.92535556_92535560del NCBI36
NG_009796.1:g.6598_6602del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370360.8:c.157_161del MANE Select ENSP00000359385.3:p.Lys53Ter
ENST00000370360.7:c.157_161del ENSP00000359385.3:p.Lys53Ter
ENST00000495106.5:c.157_161del ENSP00000436829.1:p.Lys53Ter
NM_053274.2:c.157_161del NP_444504.1:p.Lys53Ter
XM_005270400.1:c.157_161del XP_005270457.1:p.Lys53Ter
XM_005270401.2:c.39+549_39+553del XP_005270458.1:n.39+549_39+553del
XM_006710309.1:c.-369_-365del XP_006710372.1:n.-369_-365del
XM_011540544.1:c.157_161del XP_011538846.1:p.Lys53Ter
XM_011540545.1:c.157_161del XP_011538847.1:p.Lys53Ter
XM_011540546.1:c.157_161del XP_011538848.1:p.Lys53Ter
XR_946529.1:n.272_276del
NM_001319683.1:c.157_161del NP_001306612.1:p.Lys53Ter
NR_135089.1:n.272_276del
XM_005270401.3:c.39+549_39+553del XP_005270458.1:n.39+549_39+553del
XM_006710309.2:c.-369_-365del XP_006710372.1:n.-369_-365del
XM_011540546.2:c.157_161del XP_011538848.1:p.Lys53Ter
XM_017000137.1:c.256_260del XP_016855626.1:p.Lys86Ter
XM_017000138.1:c.256_260del XP_016855627.1:p.Lys86Ter
XM_017000139.1:c.256_260del XP_016855628.1:p.Lys86Ter
XM_017000140.1:c.138+549_138+553del XP_016855629.1:n.138+549_138+553del
XM_017000141.1:c.157_161del XP_016855630.1:p.Lys53Ter
XM_017000142.1:c.-369_-365del XP_016855631.1:n.-369_-365del
XM_017000143.1:c.-369_-365del XP_016855632.1:n.-369_-365del
XM_017000144.1:c.-536_-532del XP_016855633.1:n.-536_-532del
XR_002959248.1:n.640_644del
XR_002959249.1:n.272_276del
NM_053274.3:c.157_161del MANE Select NP_444504.1:p.Lys53Ter
NM_001319683.2:c.157_161del NP_001306612.1:p.Lys53Ter
NR_135089.2:n.250_254del