Canonical Allele Identifier: CA2646571984

Gene: GLMN

Linked Data

• gnomAD v4: 1-92266589-ACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266593_92266595del , CM000663.2:g.92266593_92266595del	GRCh38
NC_000001.10:g.92732150_92732152del , CM000663.1:g.92732150_92732152del	GRCh37
NC_000001.9:g.92504738_92504740del	NCBI36
NG_009796.1:g.37418_37420del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1141-100_1141-98del MANE Select	ENSP00000359385.3:n.1141-100_1141-98del
ENST00000370360.7:c.1141-100_1141-98del	ENSP00000359385.3:n.1141-100_1141-98del
ENST00000463560.1:c.510_512del
ENST00000495106.5:c.1141-100_1141-98del	ENSP00000436829.1:n.1141-100_1141-98del
ENST00000495852.6:c.364-100_364-98del	ENSP00000469157.2:n.364-100_364-98del
NM_053274.2:c.1141-100_1141-98del	NP_444504.1:n.1141-100_1141-98del
XM_005270400.1:c.1099-100_1099-98del	XP_005270457.1:n.1099-100_1099-98del
XM_005270401.2:c.1015-100_1015-98del	XP_005270458.1:n.1015-100_1015-98del
XM_006710309.1:c.640-100_640-98del	XP_006710372.1:n.640-100_640-98del
XM_011540544.1:c.1141-100_1141-98del	XP_011538846.1:n.1141-100_1141-98del
XM_011540545.1:c.1141-100_1141-98del	XP_011538847.1:n.1141-100_1141-98del
XM_011540546.1:c.1141-100_1141-98del	XP_011538848.1:n.1141-100_1141-98del
XR_946529.1:n.1257_1259del
NM_001319683.1:c.1099-100_1099-98del	NP_001306612.1:n.1099-100_1099-98del
NR_135089.1:n.1256-100_1256-98del
XM_005270401.3:c.1015-100_1015-98del	XP_005270458.1:n.1015-100_1015-98del
XM_006710309.2:c.640-100_640-98del	XP_006710372.1:n.640-100_640-98del
XM_011540546.2:c.1141-100_1141-98del	XP_011538848.1:n.1141-100_1141-98del
XM_017000137.1:c.1240-100_1240-98del	XP_016855626.1:n.1240-100_1240-98del
XM_017000138.1:c.1198-100_1198-98del	XP_016855627.1:n.1198-100_1198-98del
XM_017000139.1:c.1241_1243del
XM_017000140.1:c.1114-100_1114-98del	XP_016855629.1:n.1114-100_1114-98del
XM_017000141.1:c.1142_1144del
XM_017000142.1:c.598-100_598-98del	XP_016855631.1:n.598-100_598-98del
XM_017000143.1:c.598-100_598-98del	XP_016855632.1:n.598-100_598-98del
XM_017000144.1:c.370-100_370-98del	XP_016855633.1:n.370-100_370-98del
XR_002959248.1:n.1625_1627del
XR_002959249.1:n.1257_1259del
NM_053274.3:c.1141-100_1141-98del MANE Select	NP_444504.1:n.1141-100_1141-98del
NM_001319683.2:c.1099-100_1099-98del	NP_001306612.1:n.1099-100_1099-98del
NR_135089.2:n.1234-100_1234-98del