Canonical Allele Identifier: CA950353

Gene: GLMN

Linked Data

• dbSNP Id: rs754877795
• ExAC: 1:92732156 TA / T
• gnomAD v2: 1-92732156-TA-T
• gnomAD v3: 1-92266599-TA-T
• gnomAD v4: 1-92266599-TA-T
• MyVariant Identifiers: chr1:g.92732157del (hg19) ; chr1:g.92266600del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266604del , CM000663.2:g.92266604del	GRCh38
NC_000001.10:g.92732161del , CM000663.1:g.92732161del	GRCh37
NC_000001.9:g.92504749del	NCBI36
NG_009796.1:g.37410del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1140+100del MANE Select	ENSP00000359385.3:n.1140+100del
ENST00000370360.7:c.1140+100del	ENSP00000359385.3:n.1140+100del
ENST00000463560.1:c.509-7del
ENST00000495106.5:c.1140+100del	ENSP00000436829.1:n.1140+100del
ENST00000495852.6:c.364-108del	ENSP00000469157.2:n.364-108del
NM_053274.2:c.1140+100del	NP_444504.1:n.1140+100del
XM_005270400.1:c.1099-108del	XP_005270457.1:n.1099-108del
XM_005270401.2:c.1014+100del	XP_005270458.1:n.1014+100del
XM_006710309.1:c.639+100del	XP_006710372.1:n.639+100del
XM_011540544.1:c.1140+100del	XP_011538846.1:n.1140+100del
XM_011540545.1:c.1140+100del	XP_011538847.1:n.1140+100del
XM_011540546.1:c.1140+100del	XP_011538848.1:n.1140+100del
XR_946529.1:n.1256-7del
NM_001319683.1:c.1099-108del	NP_001306612.1:n.1099-108del
NR_135089.1:n.1255+100del
XM_005270401.3:c.1014+100del	XP_005270458.1:n.1014+100del
XM_006710309.2:c.639+100del	XP_006710372.1:n.639+100del
XM_011540546.2:c.1140+100del	XP_011538848.1:n.1140+100del
XM_017000137.1:c.1239+100del	XP_016855626.1:n.1239+100del
XM_017000138.1:c.1198-108del	XP_016855627.1:n.1198-108del
XM_017000139.1:c.1240-7del	XP_016855628.1:n.1240-7del
XM_017000140.1:c.1113+100del	XP_016855629.1:n.1113+100del
XM_017000141.1:c.1141-7del	XP_016855630.1:n.1141-7del
XM_017000142.1:c.598-108del	XP_016855631.1:n.598-108del
XM_017000143.1:c.598-108del	XP_016855632.1:n.598-108del
XM_017000144.1:c.369+100del	XP_016855633.1:n.369+100del
XR_002959248.1:n.1624-7del
XR_002959249.1:n.1256-7del
NM_053274.3:c.1140+100del MANE Select	NP_444504.1:n.1140+100del
NM_001319683.2:c.1099-108del	NP_001306612.1:n.1099-108del
NR_135089.2:n.1233+100del