Canonical Allele Identifier: CA2646571994

Gene: GLMN

Linked Data

• gnomAD v4: 1-92266632-A-AAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266633_92266635dup , CM000663.2:g.92266633_92266635dup	GRCh38
NC_000001.10:g.92732190_92732192dup , CM000663.1:g.92732190_92732192dup	GRCh37
NC_000001.9:g.92504778_92504780dup	NCBI36
NG_009796.1:g.37375_37377dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1140+65_1140+67dup MANE Select	ENSP00000359385.3:n.1140+65_1140+67dup
ENST00000370360.7:c.1140+65_1140+67dup	ENSP00000359385.3:n.1140+65_1140+67dup
ENST00000463560.1:c.509-42_509-40dup
ENST00000495106.5:c.1140+65_1140+67dup	ENSP00000436829.1:n.1140+65_1140+67dup
ENST00000495852.6:c.364-143_364-141dup	ENSP00000469157.2:n.364-143_364-141dup
NM_053274.2:c.1140+65_1140+67dup	NP_444504.1:n.1140+65_1140+67dup
XM_005270400.1:c.1099-143_1099-141dup	XP_005270457.1:n.1099-143_1099-141dup
XM_005270401.2:c.1014+65_1014+67dup	XP_005270458.1:n.1014+65_1014+67dup
XM_006710309.1:c.639+65_639+67dup	XP_006710372.1:n.639+65_639+67dup
XM_011540544.1:c.1140+65_1140+67dup	XP_011538846.1:n.1140+65_1140+67dup
XM_011540545.1:c.1140+65_1140+67dup	XP_011538847.1:n.1140+65_1140+67dup
XM_011540546.1:c.1140+65_1140+67dup	XP_011538848.1:n.1140+65_1140+67dup
XR_946529.1:n.1256-42_1256-40dup
NM_001319683.1:c.1099-143_1099-141dup	NP_001306612.1:n.1099-143_1099-141dup
NR_135089.1:n.1255+65_1255+67dup
XM_005270401.3:c.1014+65_1014+67dup	XP_005270458.1:n.1014+65_1014+67dup
XM_006710309.2:c.639+65_639+67dup	XP_006710372.1:n.639+65_639+67dup
XM_011540546.2:c.1140+65_1140+67dup	XP_011538848.1:n.1140+65_1140+67dup
XM_017000137.1:c.1239+65_1239+67dup	XP_016855626.1:n.1239+65_1239+67dup
XM_017000138.1:c.1198-143_1198-141dup	XP_016855627.1:n.1198-143_1198-141dup
XM_017000139.1:c.1240-42_1240-40dup	XP_016855628.1:n.1240-42_1240-40dup
XM_017000140.1:c.1113+65_1113+67dup	XP_016855629.1:n.1113+65_1113+67dup
XM_017000141.1:c.1141-42_1141-40dup	XP_016855630.1:n.1141-42_1141-40dup
XM_017000142.1:c.598-143_598-141dup	XP_016855631.1:n.598-143_598-141dup
XM_017000143.1:c.598-143_598-141dup	XP_016855632.1:n.598-143_598-141dup
XM_017000144.1:c.369+65_369+67dup	XP_016855633.1:n.369+65_369+67dup
XR_002959248.1:n.1624-42_1624-40dup
XR_002959249.1:n.1256-42_1256-40dup
NM_053274.3:c.1140+65_1140+67dup MANE Select	NP_444504.1:n.1140+65_1140+67dup
NM_001319683.2:c.1099-143_1099-141dup	NP_001306612.1:n.1099-143_1099-141dup
NR_135089.2:n.1233+65_1233+67dup