Canonical Allele Identifier: CA1180698734

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266077_92266078delinsAC , CM000663.2:g.92266077_92266078delinsAC	GRCh38
NC_000001.10:g.92731634_92731635delinsAC , CM000663.1:g.92731634_92731635delinsAC	GRCh37
NC_000001.9:g.92504222_92504223delinsAC	NCBI36
NG_009796.1:g.37932_37933delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1214+341_1214+342delinsGT MANE Select	ENSP00000359385.3:n.1214+341_1214+342delinsGT
ENST00000370360.7:c.1214+341_1214+342delinsGT	ENSP00000359385.3:n.1214+341_1214+342delinsGT
ENST00000463560.1:c.562+462_562+463delinsGT
ENST00000495106.5:c.1214+341_1214+342delinsGT	ENSP00000436829.1:n.1214+341_1214+342delinsGT
ENST00000495852.6:c.437+341_437+342delinsGT	ENSP00000469157.2:n.437+341_437+342delinsGT
NM_053274.2:c.1214+341_1214+342delinsGT	NP_444504.1:n.1214+341_1214+342delinsGT
XM_005270400.1:c.1172+341_1172+342delinsGT	XP_005270457.1:n.1172+341_1172+342delinsGT
XM_005270401.2:c.1088+341_1088+342delinsGT	XP_005270458.1:n.1088+341_1088+342delinsGT
XM_006710309.1:c.713+341_713+342delinsGT	XP_006710372.1:n.713+341_713+342delinsGT
XM_011540544.1:c.1214+341_1214+342delinsGT	XP_011538846.1:n.1214+341_1214+342delinsGT
XM_011540545.1:c.1214+341_1214+342delinsGT	XP_011538847.1:n.1214+341_1214+342delinsGT
XM_011540546.1:c.1214+341_1214+342delinsGT	XP_011538848.1:n.1214+341_1214+342delinsGT
XR_946529.1:n.1309+462_1309+463delinsGT
NM_001319683.1:c.1172+341_1172+342delinsGT	NP_001306612.1:n.1172+341_1172+342delinsGT
NR_135089.1:n.1329+341_1329+342delinsGT
XM_005270401.3:c.1088+341_1088+342delinsGT	XP_005270458.1:n.1088+341_1088+342delinsGT
XM_006710309.2:c.713+341_713+342delinsGT	XP_006710372.1:n.713+341_713+342delinsGT
XM_011540546.2:c.1214+341_1214+342delinsGT	XP_011538848.1:n.1214+341_1214+342delinsGT
XM_017000137.1:c.1313+341_1313+342delinsGT	XP_016855626.1:n.1313+341_1313+342delinsGT
XM_017000138.1:c.1271+341_1271+342delinsGT	XP_016855627.1:n.1271+341_1271+342delinsGT
XM_017000139.1:c.1293+462_1293+463delinsGT	XP_016855628.1:n.1293+462_1293+463delinsGT
XM_017000140.1:c.1187+341_1187+342delinsGT	XP_016855629.1:n.1187+341_1187+342delinsGT
XM_017000141.1:c.1194+462_1194+463delinsGT	XP_016855630.1:n.1194+462_1194+463delinsGT
XM_017000142.1:c.671+341_671+342delinsGT	XP_016855631.1:n.671+341_671+342delinsGT
XM_017000143.1:c.671+341_671+342delinsGT	XP_016855632.1:n.671+341_671+342delinsGT
XM_017000144.1:c.443+341_443+342delinsGT	XP_016855633.1:n.443+341_443+342delinsGT
XR_002959248.1:n.1677+462_1677+463delinsGT
XR_002959249.1:n.1309+462_1309+463delinsGT
NM_053274.3:c.1214+341_1214+342delinsGT MANE Select	NP_444504.1:n.1214+341_1214+342delinsGT
NM_001319683.2:c.1172+341_1172+342delinsGT	NP_001306612.1:n.1172+341_1172+342delinsGT
NR_135089.2:n.1307+341_1307+342delinsGT