Canonical Allele Identifier: CA740357162

Gene: GLMN

Linked Data

• dbSNP Id: rs1255187458
• gnomAD v4: 1-92266584-CT-C
• MyVariant Identifiers: chr1:g.92732142del (hg19) ; chr1:g.92266585del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266586del , CM000663.2:g.92266586del	GRCh38
NC_000001.10:g.92732143del , CM000663.1:g.92732143del	GRCh37
NC_000001.9:g.92504731del	NCBI36
NG_009796.1:g.37425del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1141-93del MANE Select	ENSP00000359385.3:n.1141-93del
ENST00000370360.7:c.1141-93del	ENSP00000359385.3:n.1141-93del
ENST00000463560.1:c.517del
ENST00000495106.5:c.1141-93del	ENSP00000436829.1:n.1141-93del
ENST00000495852.6:c.364-93del	ENSP00000469157.2:n.364-93del
NM_053274.2:c.1141-93del	NP_444504.1:n.1141-93del
XM_005270400.1:c.1099-93del	XP_005270457.1:n.1099-93del
XM_005270401.2:c.1015-93del	XP_005270458.1:n.1015-93del
XM_006710309.1:c.640-93del	XP_006710372.1:n.640-93del
XM_011540544.1:c.1141-93del	XP_011538846.1:n.1141-93del
XM_011540545.1:c.1141-93del	XP_011538847.1:n.1141-93del
XM_011540546.1:c.1141-93del	XP_011538848.1:n.1141-93del
XR_946529.1:n.1264del
NM_001319683.1:c.1099-93del	NP_001306612.1:n.1099-93del
NR_135089.1:n.1256-93del
XM_005270401.3:c.1015-93del	XP_005270458.1:n.1015-93del
XM_006710309.2:c.640-93del	XP_006710372.1:n.640-93del
XM_011540546.2:c.1141-93del	XP_011538848.1:n.1141-93del
XM_017000137.1:c.1240-93del	XP_016855626.1:n.1240-93del
XM_017000138.1:c.1198-93del	XP_016855627.1:n.1198-93del
XM_017000139.1:c.1248del	XP_016855628.1:p.Val417CysfsTer28
XM_017000140.1:c.1114-93del	XP_016855629.1:n.1114-93del
XM_017000141.1:c.1149del	XP_016855630.1:p.Val384CysfsTer28
XM_017000142.1:c.598-93del	XP_016855631.1:n.598-93del
XM_017000143.1:c.598-93del	XP_016855632.1:n.598-93del
XM_017000144.1:c.370-93del	XP_016855633.1:n.370-93del
XR_002959248.1:n.1632del
XR_002959249.1:n.1264del
NM_053274.3:c.1141-93del MANE Select	NP_444504.1:n.1141-93del
NM_001319683.2:c.1099-93del	NP_001306612.1:n.1099-93del
NR_135089.2:n.1234-93del