Canonical Allele Identifier: CA524361628

Gene: GLMN

Linked Data

• dbSNP Id: rs1178793011
• gnomAD v2: 1-92732188-AAAATT-A
• gnomAD v3: 1-92266631-AAAATT-A
• gnomAD v4: 1-92266631-AAAATT-A
• MyVariant Identifiers: chr1:g.92732189_92732193del (hg19) ; chr1:g.92266632_92266636del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266638_92266642del , CM000663.2:g.92266638_92266642del	GRCh38
NC_000001.10:g.92732195_92732199del , CM000663.1:g.92732195_92732199del	GRCh37
NC_000001.9:g.92504783_92504787del	NCBI36
NG_009796.1:g.37374_37378del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1140+64_1140+68del MANE Select	ENSP00000359385.3:n.1140+64_1140+68del
ENST00000370360.7:c.1140+64_1140+68del	ENSP00000359385.3:n.1140+64_1140+68del
ENST00000463560.1:c.509-43_509-39del
ENST00000495106.5:c.1140+64_1140+68del	ENSP00000436829.1:n.1140+64_1140+68del
ENST00000495852.6:c.364-144_364-140del	ENSP00000469157.2:n.364-144_364-140del
NM_053274.2:c.1140+64_1140+68del	NP_444504.1:n.1140+64_1140+68del
XM_005270400.1:c.1099-144_1099-140del	XP_005270457.1:n.1099-144_1099-140del
XM_005270401.2:c.1014+64_1014+68del	XP_005270458.1:n.1014+64_1014+68del
XM_006710309.1:c.639+64_639+68del	XP_006710372.1:n.639+64_639+68del
XM_011540544.1:c.1140+64_1140+68del	XP_011538846.1:n.1140+64_1140+68del
XM_011540545.1:c.1140+64_1140+68del	XP_011538847.1:n.1140+64_1140+68del
XM_011540546.1:c.1140+64_1140+68del	XP_011538848.1:n.1140+64_1140+68del
XR_946529.1:n.1256-43_1256-39del
NM_001319683.1:c.1099-144_1099-140del	NP_001306612.1:n.1099-144_1099-140del
NR_135089.1:n.1255+64_1255+68del
XM_005270401.3:c.1014+64_1014+68del	XP_005270458.1:n.1014+64_1014+68del
XM_006710309.2:c.639+64_639+68del	XP_006710372.1:n.639+64_639+68del
XM_011540546.2:c.1140+64_1140+68del	XP_011538848.1:n.1140+64_1140+68del
XM_017000137.1:c.1239+64_1239+68del	XP_016855626.1:n.1239+64_1239+68del
XM_017000138.1:c.1198-144_1198-140del	XP_016855627.1:n.1198-144_1198-140del
XM_017000139.1:c.1240-43_1240-39del	XP_016855628.1:n.1240-43_1240-39del
XM_017000140.1:c.1113+64_1113+68del	XP_016855629.1:n.1113+64_1113+68del
XM_017000141.1:c.1141-43_1141-39del	XP_016855630.1:n.1141-43_1141-39del
XM_017000142.1:c.598-144_598-140del	XP_016855631.1:n.598-144_598-140del
XM_017000143.1:c.598-144_598-140del	XP_016855632.1:n.598-144_598-140del
XM_017000144.1:c.369+64_369+68del	XP_016855633.1:n.369+64_369+68del
XR_002959248.1:n.1624-43_1624-39del
XR_002959249.1:n.1256-43_1256-39del
NM_053274.3:c.1140+64_1140+68del MANE Select	NP_444504.1:n.1140+64_1140+68del
NM_001319683.2:c.1099-144_1099-140del	NP_001306612.1:n.1099-144_1099-140del
NR_135089.2:n.1233+64_1233+68del