Canonical Allele Identifier: CA1180698717

Gene: GLMN

Linked Data

• dbSNP Id: rs1655595690

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266014_92266015insT , CM000663.2:g.92266014_92266015insT	GRCh38
NC_000001.10:g.92731571_92731572insT , CM000663.1:g.92731571_92731572insT	GRCh37
NC_000001.9:g.92504159_92504160insT	NCBI36
NG_009796.1:g.37995_37996insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1214+404_1214+405insA MANE Select	ENSP00000359385.3:n.1214+404_1214+405insA
ENST00000370360.7:c.1214+404_1214+405insA	ENSP00000359385.3:n.1214+404_1214+405insA
ENST00000463560.1:c.562+525_562+526insA
ENST00000495106.5:c.1214+404_1214+405insA	ENSP00000436829.1:n.1214+404_1214+405insA
ENST00000495852.6:c.437+404_437+405insA	ENSP00000469157.2:n.437+404_437+405insA
NM_053274.2:c.1214+404_1214+405insA	NP_444504.1:n.1214+404_1214+405insA
XM_005270400.1:c.1172+404_1172+405insA	XP_005270457.1:n.1172+404_1172+405insA
XM_005270401.2:c.1088+404_1088+405insA	XP_005270458.1:n.1088+404_1088+405insA
XM_006710309.1:c.713+404_713+405insA	XP_006710372.1:n.713+404_713+405insA
XM_011540544.1:c.1214+404_1214+405insA	XP_011538846.1:n.1214+404_1214+405insA
XM_011540545.1:c.1214+404_1214+405insA	XP_011538847.1:n.1214+404_1214+405insA
XM_011540546.1:c.1214+404_1214+405insA	XP_011538848.1:n.1214+404_1214+405insA
XR_946529.1:n.1309+525_1309+526insA
NM_001319683.1:c.1172+404_1172+405insA	NP_001306612.1:n.1172+404_1172+405insA
NR_135089.1:n.1329+404_1329+405insA
XM_005270401.3:c.1088+404_1088+405insA	XP_005270458.1:n.1088+404_1088+405insA
XM_006710309.2:c.713+404_713+405insA	XP_006710372.1:n.713+404_713+405insA
XM_011540546.2:c.1214+404_1214+405insA	XP_011538848.1:n.1214+404_1214+405insA
XM_017000137.1:c.1313+404_1313+405insA	XP_016855626.1:n.1313+404_1313+405insA
XM_017000138.1:c.1271+404_1271+405insA	XP_016855627.1:n.1271+404_1271+405insA
XM_017000139.1:c.1293+525_1293+526insA	XP_016855628.1:n.1293+525_1293+526insA
XM_017000140.1:c.1187+404_1187+405insA	XP_016855629.1:n.1187+404_1187+405insA
XM_017000141.1:c.1194+525_1194+526insA	XP_016855630.1:n.1194+525_1194+526insA
XM_017000142.1:c.671+404_671+405insA	XP_016855631.1:n.671+404_671+405insA
XM_017000143.1:c.671+404_671+405insA	XP_016855632.1:n.671+404_671+405insA
XM_017000144.1:c.443+404_443+405insA	XP_016855633.1:n.443+404_443+405insA
XR_002959248.1:n.1677+525_1677+526insA
XR_002959249.1:n.1309+525_1309+526insA
NM_053274.3:c.1214+404_1214+405insA MANE Select	NP_444504.1:n.1214+404_1214+405insA
NM_001319683.2:c.1172+404_1172+405insA	NP_001306612.1:n.1172+404_1172+405insA
NR_135089.2:n.1307+404_1307+405insA