Canonical Allele Identifier: CA1148730692
Gene: GLMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92266663_92266667delinsTAACT , CM000663.2:g.92266663_92266667delinsTAACT GRCh38
NC_000001.10:g.92732220_92732224delinsTAACT , CM000663.1:g.92732220_92732224delinsTAACT GRCh37
NC_000001.9:g.92504808_92504812delinsTAACT NCBI36
NG_009796.1:g.37343_37347delinsAGTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000370360.8:c.1140+33_1140+37delinsAGTTA MANE Select ENSP00000359385.3:n.1140+33_1140+37delinsAGTTA
ENST00000370360.7:c.1140+33_1140+37delinsAGTTA ENSP00000359385.3:n.1140+33_1140+37delinsAGTTA
ENST00000463560.1:c.508+33_508+37delinsAGTTA
ENST00000495106.5:c.1140+33_1140+37delinsAGTTA ENSP00000436829.1:n.1140+33_1140+37delinsAGTTA
ENST00000495852.6:c.364-175_364-171delinsAGTTA ENSP00000469157.2:n.364-175_364-171delinsAGTTA
NM_053274.2:c.1140+33_1140+37delinsAGTTA NP_444504.1:n.1140+33_1140+37delinsAGTTA
XM_005270400.1:c.1099-175_1099-171delinsAGTTA XP_005270457.1:n.1099-175_1099-171delinsAGTTA
XM_005270401.2:c.1014+33_1014+37delinsAGTTA XP_005270458.1:n.1014+33_1014+37delinsAGTTA
XM_006710309.1:c.639+33_639+37delinsAGTTA XP_006710372.1:n.639+33_639+37delinsAGTTA
XM_011540544.1:c.1140+33_1140+37delinsAGTTA XP_011538846.1:n.1140+33_1140+37delinsAGTTA
XM_011540545.1:c.1140+33_1140+37delinsAGTTA XP_011538847.1:n.1140+33_1140+37delinsAGTTA
XM_011540546.1:c.1140+33_1140+37delinsAGTTA XP_011538848.1:n.1140+33_1140+37delinsAGTTA
XR_946529.1:n.1255+33_1255+37delinsAGTTA
NM_001319683.1:c.1099-175_1099-171delinsAGTTA NP_001306612.1:n.1099-175_1099-171delinsAGTTA
NR_135089.1:n.1255+33_1255+37delinsAGTTA
XM_005270401.3:c.1014+33_1014+37delinsAGTTA XP_005270458.1:n.1014+33_1014+37delinsAGTTA
XM_006710309.2:c.639+33_639+37delinsAGTTA XP_006710372.1:n.639+33_639+37delinsAGTTA
XM_011540546.2:c.1140+33_1140+37delinsAGTTA XP_011538848.1:n.1140+33_1140+37delinsAGTTA
XM_017000137.1:c.1239+33_1239+37delinsAGTTA XP_016855626.1:n.1239+33_1239+37delinsAGTTA
XM_017000138.1:c.1198-175_1198-171delinsAGTTA XP_016855627.1:n.1198-175_1198-171delinsAGTTA
XM_017000139.1:c.1239+33_1239+37delinsAGTTA XP_016855628.1:n.1239+33_1239+37delinsAGTTA
XM_017000140.1:c.1113+33_1113+37delinsAGTTA XP_016855629.1:n.1113+33_1113+37delinsAGTTA
XM_017000141.1:c.1140+33_1140+37delinsAGTTA XP_016855630.1:n.1140+33_1140+37delinsAGTTA
XM_017000142.1:c.598-175_598-171delinsAGTTA XP_016855631.1:n.598-175_598-171delinsAGTTA
XM_017000143.1:c.598-175_598-171delinsAGTTA XP_016855632.1:n.598-175_598-171delinsAGTTA
XM_017000144.1:c.369+33_369+37delinsAGTTA XP_016855633.1:n.369+33_369+37delinsAGTTA
XR_002959248.1:n.1623+33_1623+37delinsAGTTA
XR_002959249.1:n.1255+33_1255+37delinsAGTTA
NM_053274.3:c.1140+33_1140+37delinsAGTTA MANE Select NP_444504.1:n.1140+33_1140+37delinsAGTTA
NM_001319683.2:c.1099-175_1099-171delinsAGTTA NP_001306612.1:n.1099-175_1099-171delinsAGTTA
NR_135089.2:n.1233+33_1233+37delinsAGTTA