Canonical Allele Identifier: CA1004437625

Gene: GLMN

Linked Data

• dbSNP Id: rs1655588929
• gnomAD v3: 1-92265954-ACCAAT-A
• gnomAD v4: 1-92265954-ACCAAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92265956_92265960del , CM000663.2:g.92265956_92265960del	GRCh38
NC_000001.10:g.92731513_92731517del , CM000663.1:g.92731513_92731517del	GRCh37
NC_000001.9:g.92504101_92504105del	NCBI36
NG_009796.1:g.38051_38055del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1214+460_1214+464del MANE Select	ENSP00000359385.3:n.1214+460_1214+464del
ENST00000370360.7:c.1214+460_1214+464del	ENSP00000359385.3:n.1214+460_1214+464del
ENST00000463560.1:c.562+581_562+585del
ENST00000495106.5:c.1214+460_1214+464del	ENSP00000436829.1:n.1214+460_1214+464del
ENST00000495852.6:c.437+460_437+464del	ENSP00000469157.2:n.437+460_437+464del
NM_053274.2:c.1214+460_1214+464del	NP_444504.1:n.1214+460_1214+464del
XM_005270400.1:c.1172+460_1172+464del	XP_005270457.1:n.1172+460_1172+464del
XM_005270401.2:c.1088+460_1088+464del	XP_005270458.1:n.1088+460_1088+464del
XM_006710309.1:c.713+460_713+464del	XP_006710372.1:n.713+460_713+464del
XM_011540544.1:c.1214+460_1214+464del	XP_011538846.1:n.1214+460_1214+464del
XM_011540545.1:c.1214+460_1214+464del	XP_011538847.1:n.1214+460_1214+464del
XM_011540546.1:c.1214+460_1214+464del	XP_011538848.1:n.1214+460_1214+464del
XR_946529.1:n.1309+581_1309+585del
NM_001319683.1:c.1172+460_1172+464del	NP_001306612.1:n.1172+460_1172+464del
NR_135089.1:n.1329+460_1329+464del
XM_005270401.3:c.1088+460_1088+464del	XP_005270458.1:n.1088+460_1088+464del
XM_006710309.2:c.713+460_713+464del	XP_006710372.1:n.713+460_713+464del
XM_011540546.2:c.1214+460_1214+464del	XP_011538848.1:n.1214+460_1214+464del
XM_017000137.1:c.1313+460_1313+464del	XP_016855626.1:n.1313+460_1313+464del
XM_017000138.1:c.1271+460_1271+464del	XP_016855627.1:n.1271+460_1271+464del
XM_017000139.1:c.1293+581_1293+585del	XP_016855628.1:n.1293+581_1293+585del
XM_017000140.1:c.1187+460_1187+464del	XP_016855629.1:n.1187+460_1187+464del
XM_017000141.1:c.1194+581_1194+585del	XP_016855630.1:n.1194+581_1194+585del
XM_017000142.1:c.671+460_671+464del	XP_016855631.1:n.671+460_671+464del
XM_017000143.1:c.671+460_671+464del	XP_016855632.1:n.671+460_671+464del
XM_017000144.1:c.443+460_443+464del	XP_016855633.1:n.443+460_443+464del
XR_002959248.1:n.1677+581_1677+585del
XR_002959249.1:n.1309+581_1309+585del
NM_053274.3:c.1214+460_1214+464del MANE Select	NP_444504.1:n.1214+460_1214+464del
NM_001319683.2:c.1172+460_1172+464del	NP_001306612.1:n.1172+460_1172+464del
NR_135089.2:n.1307+460_1307+464del