Canonical Allele Identifier: CA1180698921
Gene: GLMN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92266546T= , CM000663.2:g.92266546T= GRCh38
NC_000001.10:g.92732103T= , CM000663.1:g.92732103T= GRCh37
NC_000001.9:g.92504691T= NCBI36
NG_009796.1:g.37464A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370360.8:c.1141-54A= MANE Select ENSP00000359385.3:n.1141-54A=
ENST00000370360.7:c.1141-54A= ENSP00000359385.3:n.1141-54A=
ENST00000463560.1:c.556A=
ENST00000495106.5:c.1141-54A= ENSP00000436829.1:n.1141-54A=
ENST00000495852.6:c.364-54A= ENSP00000469157.2:n.364-54A=
NM_053274.2:c.1141-54A= NP_444504.1:n.1141-54A=
XM_005270400.1:c.1099-54A= XP_005270457.1:n.1099-54A=
XM_005270401.2:c.1015-54A= XP_005270458.1:n.1015-54A=
XM_006710309.1:c.640-54A= XP_006710372.1:n.640-54A=
XM_011540544.1:c.1141-54A= XP_011538846.1:n.1141-54A=
XM_011540545.1:c.1141-54A= XP_011538847.1:n.1141-54A=
XM_011540546.1:c.1141-54A= XP_011538848.1:n.1141-54A=
XR_946529.1:n.1303A=
NM_001319683.1:c.1099-54A= NP_001306612.1:n.1099-54A=
NR_135089.1:n.1256-54A=
XM_005270401.3:c.1015-54A= XP_005270458.1:n.1015-54A=
XM_006710309.2:c.640-54A= XP_006710372.1:n.640-54A=
XM_011540546.2:c.1141-54A= XP_011538848.1:n.1141-54A=
XM_017000137.1:c.1240-54A= XP_016855626.1:n.1240-54A=
XM_017000138.1:c.1198-54A= XP_016855627.1:n.1198-54A=
XM_017000139.1:c.1287A= XP_016855628.1:p.Glu429=
XM_017000140.1:c.1114-54A= XP_016855629.1:n.1114-54A=
XM_017000141.1:c.1188A= XP_016855630.1:p.Glu396=
XM_017000142.1:c.598-54A= XP_016855631.1:n.598-54A=
XM_017000143.1:c.598-54A= XP_016855632.1:n.598-54A=
XM_017000144.1:c.370-54A= XP_016855633.1:n.370-54A=
XR_002959248.1:n.1671A=
XR_002959249.1:n.1303A=
NM_053274.3:c.1141-54A= MANE Select NP_444504.1:n.1141-54A=
NM_001319683.2:c.1099-54A= NP_001306612.1:n.1099-54A=
NR_135089.2:n.1234-54A=