Canonical Allele Identifier: CA1180698842

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266401_92266402delinsGC , CM000663.2:g.92266401_92266402delinsGC	GRCh38
NC_000001.10:g.92731958_92731959delinsGC , CM000663.1:g.92731958_92731959delinsGC	GRCh37
NC_000001.9:g.92504546_92504547delinsGC	NCBI36
NG_009796.1:g.37608_37609delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1214+17_1214+18delinsGC MANE Select	ENSP00000359385.3:n.1214+17_1214+18delinsGC
ENST00000370360.7:c.1214+17_1214+18delinsGC	ENSP00000359385.3:n.1214+17_1214+18delinsGC
ENST00000463560.1:c.562+138_562+139delinsGC
ENST00000495106.5:c.1214+17_1214+18delinsGC	ENSP00000436829.1:n.1214+17_1214+18delinsGC
ENST00000495852.6:c.437+17_437+18delinsGC	ENSP00000469157.2:n.437+17_437+18delinsGC
NM_053274.2:c.1214+17_1214+18delinsGC	NP_444504.1:n.1214+17_1214+18delinsGC
XM_005270400.1:c.1172+17_1172+18delinsGC	XP_005270457.1:n.1172+17_1172+18delinsGC
XM_005270401.2:c.1088+17_1088+18delinsGC	XP_005270458.1:n.1088+17_1088+18delinsGC
XM_006710309.1:c.713+17_713+18delinsGC	XP_006710372.1:n.713+17_713+18delinsGC
XM_011540544.1:c.1214+17_1214+18delinsGC	XP_011538846.1:n.1214+17_1214+18delinsGC
XM_011540545.1:c.1214+17_1214+18delinsGC	XP_011538847.1:n.1214+17_1214+18delinsGC
XM_011540546.1:c.1214+17_1214+18delinsGC	XP_011538848.1:n.1214+17_1214+18delinsGC
XR_946529.1:n.1309+138_1309+139delinsGC
NM_001319683.1:c.1172+17_1172+18delinsGC	NP_001306612.1:n.1172+17_1172+18delinsGC
NR_135089.1:n.1329+17_1329+18delinsGC
XM_005270401.3:c.1088+17_1088+18delinsGC	XP_005270458.1:n.1088+17_1088+18delinsGC
XM_006710309.2:c.713+17_713+18delinsGC	XP_006710372.1:n.713+17_713+18delinsGC
XM_011540546.2:c.1214+17_1214+18delinsGC	XP_011538848.1:n.1214+17_1214+18delinsGC
XM_017000137.1:c.1313+17_1313+18delinsGC	XP_016855626.1:n.1313+17_1313+18delinsGC
XM_017000138.1:c.1271+17_1271+18delinsGC	XP_016855627.1:n.1271+17_1271+18delinsGC
XM_017000139.1:c.1293+138_1293+139delinsGC	XP_016855628.1:n.1293+138_1293+139delinsGC
XM_017000140.1:c.1187+17_1187+18delinsGC	XP_016855629.1:n.1187+17_1187+18delinsGC
XM_017000141.1:c.1194+138_1194+139delinsGC	XP_016855630.1:n.1194+138_1194+139delinsGC
XM_017000142.1:c.671+17_671+18delinsGC	XP_016855631.1:n.671+17_671+18delinsGC
XM_017000143.1:c.671+17_671+18delinsGC	XP_016855632.1:n.671+17_671+18delinsGC
XM_017000144.1:c.443+17_443+18delinsGC	XP_016855633.1:n.443+17_443+18delinsGC
XR_002959248.1:n.1677+138_1677+139delinsGC
XR_002959249.1:n.1309+138_1309+139delinsGC
NM_053274.3:c.1214+17_1214+18delinsGC MANE Select	NP_444504.1:n.1214+17_1214+18delinsGC
NM_001319683.2:c.1172+17_1172+18delinsGC	NP_001306612.1:n.1172+17_1172+18delinsGC
NR_135089.2:n.1307+17_1307+18delinsGC