Canonical Allele Identifier: CA1004437684

Gene: GLMN

Linked Data

• dbSNP Id: rs1655609748
• gnomAD v3: 1-92266167-T-TTAGAG
• gnomAD v4: 1-92266167-T-TTAGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266170_92266174dup , CM000663.2:g.92266170_92266174dup	GRCh38
NC_000001.10:g.92731727_92731731dup , CM000663.1:g.92731727_92731731dup	GRCh37
NC_000001.9:g.92504315_92504319dup	NCBI36
NG_009796.1:g.37838_37842dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1214+247_1214+251dup MANE Select	ENSP00000359385.3:n.1214+247_1214+251dup
ENST00000370360.7:c.1214+247_1214+251dup	ENSP00000359385.3:n.1214+247_1214+251dup
ENST00000463560.1:c.562+368_562+372dup
ENST00000495106.5:c.1214+247_1214+251dup	ENSP00000436829.1:n.1214+247_1214+251dup
ENST00000495852.6:c.437+247_437+251dup	ENSP00000469157.2:n.437+247_437+251dup
NM_053274.2:c.1214+247_1214+251dup	NP_444504.1:n.1214+247_1214+251dup
XM_005270400.1:c.1172+247_1172+251dup	XP_005270457.1:n.1172+247_1172+251dup
XM_005270401.2:c.1088+247_1088+251dup	XP_005270458.1:n.1088+247_1088+251dup
XM_006710309.1:c.713+247_713+251dup	XP_006710372.1:n.713+247_713+251dup
XM_011540544.1:c.1214+247_1214+251dup	XP_011538846.1:n.1214+247_1214+251dup
XM_011540545.1:c.1214+247_1214+251dup	XP_011538847.1:n.1214+247_1214+251dup
XM_011540546.1:c.1214+247_1214+251dup	XP_011538848.1:n.1214+247_1214+251dup
XR_946529.1:n.1309+368_1309+372dup
NM_001319683.1:c.1172+247_1172+251dup	NP_001306612.1:n.1172+247_1172+251dup
NR_135089.1:n.1329+247_1329+251dup
XM_005270401.3:c.1088+247_1088+251dup	XP_005270458.1:n.1088+247_1088+251dup
XM_006710309.2:c.713+247_713+251dup	XP_006710372.1:n.713+247_713+251dup
XM_011540546.2:c.1214+247_1214+251dup	XP_011538848.1:n.1214+247_1214+251dup
XM_017000137.1:c.1313+247_1313+251dup	XP_016855626.1:n.1313+247_1313+251dup
XM_017000138.1:c.1271+247_1271+251dup	XP_016855627.1:n.1271+247_1271+251dup
XM_017000139.1:c.1293+368_1293+372dup	XP_016855628.1:n.1293+368_1293+372dup
XM_017000140.1:c.1187+247_1187+251dup	XP_016855629.1:n.1187+247_1187+251dup
XM_017000141.1:c.1194+368_1194+372dup	XP_016855630.1:n.1194+368_1194+372dup
XM_017000142.1:c.671+247_671+251dup	XP_016855631.1:n.671+247_671+251dup
XM_017000143.1:c.671+247_671+251dup	XP_016855632.1:n.671+247_671+251dup
XM_017000144.1:c.443+247_443+251dup	XP_016855633.1:n.443+247_443+251dup
XR_002959248.1:n.1677+368_1677+372dup
XR_002959249.1:n.1309+368_1309+372dup
NM_053274.3:c.1214+247_1214+251dup MANE Select	NP_444504.1:n.1214+247_1214+251dup
NM_001319683.2:c.1172+247_1172+251dup	NP_001306612.1:n.1172+247_1172+251dup
NR_135089.2:n.1307+247_1307+251dup