Canonical Allele Identifier: CA1180698964

Gene: GLMN

Linked Data

• dbSNP Id: rs1655670197

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266630_92266634dup , CM000663.2:g.92266630_92266634dup	GRCh38
NC_000001.10:g.92732187_92732191dup , CM000663.1:g.92732187_92732191dup	GRCh37
NC_000001.9:g.92504775_92504779dup	NCBI36
NG_009796.1:g.37380_37384dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1140+70_1140+74dup MANE Select	ENSP00000359385.3:n.1140+70_1140+74dup
ENST00000370360.7:c.1140+70_1140+74dup	ENSP00000359385.3:n.1140+70_1140+74dup
ENST00000463560.1:c.509-37_509-33dup
ENST00000495106.5:c.1140+70_1140+74dup	ENSP00000436829.1:n.1140+70_1140+74dup
ENST00000495852.6:c.364-138_364-134dup	ENSP00000469157.2:n.364-138_364-134dup
NM_053274.2:c.1140+70_1140+74dup	NP_444504.1:n.1140+70_1140+74dup
XM_005270400.1:c.1099-138_1099-134dup	XP_005270457.1:n.1099-138_1099-134dup
XM_005270401.2:c.1014+70_1014+74dup	XP_005270458.1:n.1014+70_1014+74dup
XM_006710309.1:c.639+70_639+74dup	XP_006710372.1:n.639+70_639+74dup
XM_011540544.1:c.1140+70_1140+74dup	XP_011538846.1:n.1140+70_1140+74dup
XM_011540545.1:c.1140+70_1140+74dup	XP_011538847.1:n.1140+70_1140+74dup
XM_011540546.1:c.1140+70_1140+74dup	XP_011538848.1:n.1140+70_1140+74dup
XR_946529.1:n.1256-37_1256-33dup
NM_001319683.1:c.1099-138_1099-134dup	NP_001306612.1:n.1099-138_1099-134dup
NR_135089.1:n.1255+70_1255+74dup
XM_005270401.3:c.1014+70_1014+74dup	XP_005270458.1:n.1014+70_1014+74dup
XM_006710309.2:c.639+70_639+74dup	XP_006710372.1:n.639+70_639+74dup
XM_011540546.2:c.1140+70_1140+74dup	XP_011538848.1:n.1140+70_1140+74dup
XM_017000137.1:c.1239+70_1239+74dup	XP_016855626.1:n.1239+70_1239+74dup
XM_017000138.1:c.1198-138_1198-134dup	XP_016855627.1:n.1198-138_1198-134dup
XM_017000139.1:c.1240-37_1240-33dup	XP_016855628.1:n.1240-37_1240-33dup
XM_017000140.1:c.1113+70_1113+74dup	XP_016855629.1:n.1113+70_1113+74dup
XM_017000141.1:c.1141-37_1141-33dup	XP_016855630.1:n.1141-37_1141-33dup
XM_017000142.1:c.598-138_598-134dup	XP_016855631.1:n.598-138_598-134dup
XM_017000143.1:c.598-138_598-134dup	XP_016855632.1:n.598-138_598-134dup
XM_017000144.1:c.369+70_369+74dup	XP_016855633.1:n.369+70_369+74dup
XR_002959248.1:n.1624-37_1624-33dup
XR_002959249.1:n.1256-37_1256-33dup
NM_053274.3:c.1140+70_1140+74dup MANE Select	NP_444504.1:n.1140+70_1140+74dup
NM_001319683.2:c.1099-138_1099-134dup	NP_001306612.1:n.1099-138_1099-134dup
NR_135089.2:n.1233+70_1233+74dup