Canonical Allele Identifier: CA2744569905

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266323_92266324dup , CM000663.2:g.92266323_92266324dup	GRCh38
NC_000001.10:g.92731880_92731881dup , CM000663.1:g.92731880_92731881dup	GRCh37
NC_000001.9:g.92504468_92504469dup	NCBI36
NG_009796.1:g.37688_37689dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1214+97_1214+98dup MANE Select	ENSP00000359385.3:n.1214+97_1214+98dup
ENST00000370360.7:c.1214+97_1214+98dup	ENSP00000359385.3:n.1214+97_1214+98dup
ENST00000463560.1:c.562+218_562+219dup
ENST00000495106.5:c.1214+97_1214+98dup	ENSP00000436829.1:n.1214+97_1214+98dup
ENST00000495852.6:c.437+97_437+98dup	ENSP00000469157.2:n.437+97_437+98dup
NM_053274.2:c.1214+97_1214+98dup	NP_444504.1:n.1214+97_1214+98dup
XM_005270400.1:c.1172+97_1172+98dup	XP_005270457.1:n.1172+97_1172+98dup
XM_005270401.2:c.1088+97_1088+98dup	XP_005270458.1:n.1088+97_1088+98dup
XM_006710309.1:c.713+97_713+98dup	XP_006710372.1:n.713+97_713+98dup
XM_011540544.1:c.1214+97_1214+98dup	XP_011538846.1:n.1214+97_1214+98dup
XM_011540545.1:c.1214+97_1214+98dup	XP_011538847.1:n.1214+97_1214+98dup
XM_011540546.1:c.1214+97_1214+98dup	XP_011538848.1:n.1214+97_1214+98dup
XR_946529.1:n.1309+218_1309+219dup
NM_001319683.1:c.1172+97_1172+98dup	NP_001306612.1:n.1172+97_1172+98dup
NR_135089.1:n.1329+97_1329+98dup
XM_005270401.3:c.1088+97_1088+98dup	XP_005270458.1:n.1088+97_1088+98dup
XM_006710309.2:c.713+97_713+98dup	XP_006710372.1:n.713+97_713+98dup
XM_011540546.2:c.1214+97_1214+98dup	XP_011538848.1:n.1214+97_1214+98dup
XM_017000137.1:c.1313+97_1313+98dup	XP_016855626.1:n.1313+97_1313+98dup
XM_017000138.1:c.1271+97_1271+98dup	XP_016855627.1:n.1271+97_1271+98dup
XM_017000139.1:c.1293+218_1293+219dup	XP_016855628.1:n.1293+218_1293+219dup
XM_017000140.1:c.1187+97_1187+98dup	XP_016855629.1:n.1187+97_1187+98dup
XM_017000141.1:c.1194+218_1194+219dup	XP_016855630.1:n.1194+218_1194+219dup
XM_017000142.1:c.671+97_671+98dup	XP_016855631.1:n.671+97_671+98dup
XM_017000143.1:c.671+97_671+98dup	XP_016855632.1:n.671+97_671+98dup
XM_017000144.1:c.443+97_443+98dup	XP_016855633.1:n.443+97_443+98dup
XR_002959248.1:n.1677+218_1677+219dup
XR_002959249.1:n.1309+218_1309+219dup
NM_053274.3:c.1214+97_1214+98dup MANE Select	NP_444504.1:n.1214+97_1214+98dup
NM_001319683.2:c.1172+97_1172+98dup	NP_001306612.1:n.1172+97_1172+98dup
NR_135089.2:n.1307+97_1307+98dup