Canonical Allele Identifier: CA950352

Gene: GLMN

Linked Data

• dbSNP Id: rs751344286
• ExAC: 1:92732151 CTAAA / C
• gnomAD v2: 1-92732151-CTAAA-C
• gnomAD v3: 1-92266594-CTAAA-C
• gnomAD v4: 1-92266594-CTAAA-C
• MyVariant Identifiers: chr1:g.92732152_92732155del (hg19) ; chr1:g.92266595_92266598del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266599_92266602del , CM000663.2:g.92266599_92266602del	GRCh38
NC_000001.10:g.92732156_92732159del , CM000663.1:g.92732156_92732159del	GRCh37
NC_000001.9:g.92504744_92504747del	NCBI36
NG_009796.1:g.37412_37415del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1140+102_1141-103del MANE Select	ENSP00000359385.3:n.1140+102_1141-103del
ENST00000370360.7:c.1140+102_1141-103del	ENSP00000359385.3:n.1140+102_1141-103del
ENST00000463560.1:c.509-5_509-2del
ENST00000495106.5:c.1140+102_1141-103del	ENSP00000436829.1:n.1140+102_1141-103del
ENST00000495852.6:c.364-106_364-103del	ENSP00000469157.2:n.364-106_364-103del
NM_053274.2:c.1140+102_1141-103del	NP_444504.1:n.1140+102_1141-103del
XM_005270400.1:c.1099-106_1099-103del	XP_005270457.1:n.1099-106_1099-103del
XM_005270401.2:c.1014+102_1015-103del	XP_005270458.1:n.1014+102_1015-103del
XM_006710309.1:c.639+102_640-103del	XP_006710372.1:n.639+102_640-103del
XM_011540544.1:c.1140+102_1141-103del	XP_011538846.1:n.1140+102_1141-103del
XM_011540545.1:c.1140+102_1141-103del	XP_011538847.1:n.1140+102_1141-103del
XM_011540546.1:c.1140+102_1141-103del	XP_011538848.1:n.1140+102_1141-103del
XR_946529.1:n.1256-5_1256-2del
NM_001319683.1:c.1099-106_1099-103del	NP_001306612.1:n.1099-106_1099-103del
NR_135089.1:n.1255+102_1256-103del
XM_005270401.3:c.1014+102_1015-103del	XP_005270458.1:n.1014+102_1015-103del
XM_006710309.2:c.639+102_640-103del	XP_006710372.1:n.639+102_640-103del
XM_011540546.2:c.1140+102_1141-103del	XP_011538848.1:n.1140+102_1141-103del
XM_017000137.1:c.1239+102_1240-103del	XP_016855626.1:n.1239+102_1240-103del
XM_017000138.1:c.1198-106_1198-103del	XP_016855627.1:n.1198-106_1198-103del
XM_017000139.1:c.1240-5_1240-2del	XP_016855628.1:n.1240-5_1240-2del
XM_017000140.1:c.1113+102_1114-103del	XP_016855629.1:n.1113+102_1114-103del
XM_017000141.1:c.1141-5_1141-2del	XP_016855630.1:n.1141-5_1141-2del
XM_017000142.1:c.598-106_598-103del	XP_016855631.1:n.598-106_598-103del
XM_017000143.1:c.598-106_598-103del	XP_016855632.1:n.598-106_598-103del
XM_017000144.1:c.369+102_370-103del	XP_016855633.1:n.369+102_370-103del
XR_002959248.1:n.1624-5_1624-2del
XR_002959249.1:n.1256-5_1256-2del
NM_053274.3:c.1140+102_1141-103del MANE Select	NP_444504.1:n.1140+102_1141-103del
NM_001319683.2:c.1099-106_1099-103del	NP_001306612.1:n.1099-106_1099-103del
NR_135089.2:n.1233+102_1234-103del