Canonical Allele Identifier: CA2646571978

Gene: GLMN

Linked Data

• gnomAD v4: 1-92266576-C-CAAATGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266577_92266578insAATGTA , CM000663.2:g.92266577_92266578insAATGTA	GRCh38
NC_000001.10:g.92732134_92732135insAATGTA , CM000663.1:g.92732134_92732135insAATGTA	GRCh37
NC_000001.9:g.92504722_92504723insAATGTA	NCBI36
NG_009796.1:g.37433_37434insACATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1141-85_1141-84insACATTT MANE Select	ENSP00000359385.3:n.1141-85_1141-84insACATTT
ENST00000370360.7:c.1141-85_1141-84insACATTT	ENSP00000359385.3:n.1141-85_1141-84insACATTT
ENST00000463560.1:c.525_526insACATTT
ENST00000495106.5:c.1141-85_1141-84insACATTT	ENSP00000436829.1:n.1141-85_1141-84insACATTT
ENST00000495852.6:c.364-85_364-84insACATTT	ENSP00000469157.2:n.364-85_364-84insACATTT
NM_053274.2:c.1141-85_1141-84insACATTT	NP_444504.1:n.1141-85_1141-84insACATTT
XM_005270400.1:c.1099-85_1099-84insACATTT	XP_005270457.1:n.1099-85_1099-84insACATTT
XM_005270401.2:c.1015-85_1015-84insACATTT	XP_005270458.1:n.1015-85_1015-84insACATTT
XM_006710309.1:c.640-85_640-84insACATTT	XP_006710372.1:n.640-85_640-84insACATTT
XM_011540544.1:c.1141-85_1141-84insACATTT	XP_011538846.1:n.1141-85_1141-84insACATTT
XM_011540545.1:c.1141-85_1141-84insACATTT	XP_011538847.1:n.1141-85_1141-84insACATTT
XM_011540546.1:c.1141-85_1141-84insACATTT	XP_011538848.1:n.1141-85_1141-84insACATTT
XR_946529.1:n.1272_1273insACATTT
NM_001319683.1:c.1099-85_1099-84insACATTT	NP_001306612.1:n.1099-85_1099-84insACATTT
NR_135089.1:n.1256-85_1256-84insACATTT
XM_005270401.3:c.1015-85_1015-84insACATTT	XP_005270458.1:n.1015-85_1015-84insACATTT
XM_006710309.2:c.640-85_640-84insACATTT	XP_006710372.1:n.640-85_640-84insACATTT
XM_011540546.2:c.1141-85_1141-84insACATTT	XP_011538848.1:n.1141-85_1141-84insACATTT
XM_017000137.1:c.1240-85_1240-84insACATTT	XP_016855626.1:n.1240-85_1240-84insACATTT
XM_017000138.1:c.1198-85_1198-84insACATTT	XP_016855627.1:n.1198-85_1198-84insACATTT
XM_017000139.1:c.1256_1257insACATTT	XP_016855628.1:p.Met419delinsIleHisLeu
XM_017000140.1:c.1114-85_1114-84insACATTT	XP_016855629.1:n.1114-85_1114-84insACATTT
XM_017000141.1:c.1157_1158insACATTT	XP_016855630.1:p.Met386delinsIleHisLeu
XM_017000142.1:c.598-85_598-84insACATTT	XP_016855631.1:n.598-85_598-84insACATTT
XM_017000143.1:c.598-85_598-84insACATTT	XP_016855632.1:n.598-85_598-84insACATTT
XM_017000144.1:c.370-85_370-84insACATTT	XP_016855633.1:n.370-85_370-84insACATTT
XR_002959248.1:n.1640_1641insACATTT
XR_002959249.1:n.1272_1273insACATTT
NM_053274.3:c.1141-85_1141-84insACATTT MANE Select	NP_444504.1:n.1141-85_1141-84insACATTT
NM_001319683.2:c.1099-85_1099-84insACATTT	NP_001306612.1:n.1099-85_1099-84insACATTT
NR_135089.2:n.1234-85_1234-84insACATTT