Canonical Allele Identifier: CA1180698698

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92265968_92265972delinsTAGAG , CM000663.2:g.92265968_92265972delinsTAGAG	GRCh38
NC_000001.10:g.92731525_92731529delinsTAGAG , CM000663.1:g.92731525_92731529delinsTAGAG	GRCh37
NC_000001.9:g.92504113_92504117delinsTAGAG	NCBI36
NG_009796.1:g.38038_38042delinsCTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1214+447_1214+451delinsCTCTA MANE Select	ENSP00000359385.3:n.1214+447_1214+451delinsCTCTA
ENST00000370360.7:c.1214+447_1214+451delinsCTCTA	ENSP00000359385.3:n.1214+447_1214+451delinsCTCTA
ENST00000463560.1:c.562+568_562+572delinsCTCTA
ENST00000495106.5:c.1214+447_1214+451delinsCTCTA	ENSP00000436829.1:n.1214+447_1214+451delinsCTCTA
ENST00000495852.6:c.437+447_437+451delinsCTCTA	ENSP00000469157.2:n.437+447_437+451delinsCTCTA
NM_053274.2:c.1214+447_1214+451delinsCTCTA	NP_444504.1:n.1214+447_1214+451delinsCTCTA
XM_005270400.1:c.1172+447_1172+451delinsCTCTA	XP_005270457.1:n.1172+447_1172+451delinsCTCTA
XM_005270401.2:c.1088+447_1088+451delinsCTCTA	XP_005270458.1:n.1088+447_1088+451delinsCTCTA
XM_006710309.1:c.713+447_713+451delinsCTCTA	XP_006710372.1:n.713+447_713+451delinsCTCTA
XM_011540544.1:c.1214+447_1214+451delinsCTCTA	XP_011538846.1:n.1214+447_1214+451delinsCTCTA
XM_011540545.1:c.1214+447_1214+451delinsCTCTA	XP_011538847.1:n.1214+447_1214+451delinsCTCTA
XM_011540546.1:c.1214+447_1214+451delinsCTCTA	XP_011538848.1:n.1214+447_1214+451delinsCTCTA
XR_946529.1:n.1309+568_1309+572delinsCTCTA
NM_001319683.1:c.1172+447_1172+451delinsCTCTA	NP_001306612.1:n.1172+447_1172+451delinsCTCTA
NR_135089.1:n.1329+447_1329+451delinsCTCTA
XM_005270401.3:c.1088+447_1088+451delinsCTCTA	XP_005270458.1:n.1088+447_1088+451delinsCTCTA
XM_006710309.2:c.713+447_713+451delinsCTCTA	XP_006710372.1:n.713+447_713+451delinsCTCTA
XM_011540546.2:c.1214+447_1214+451delinsCTCTA	XP_011538848.1:n.1214+447_1214+451delinsCTCTA
XM_017000137.1:c.1313+447_1313+451delinsCTCTA	XP_016855626.1:n.1313+447_1313+451delinsCTCTA
XM_017000138.1:c.1271+447_1271+451delinsCTCTA	XP_016855627.1:n.1271+447_1271+451delinsCTCTA
XM_017000139.1:c.1293+568_1293+572delinsCTCTA	XP_016855628.1:n.1293+568_1293+572delinsCTCTA
XM_017000140.1:c.1187+447_1187+451delinsCTCTA	XP_016855629.1:n.1187+447_1187+451delinsCTCTA
XM_017000141.1:c.1194+568_1194+572delinsCTCTA	XP_016855630.1:n.1194+568_1194+572delinsCTCTA
XM_017000142.1:c.671+447_671+451delinsCTCTA	XP_016855631.1:n.671+447_671+451delinsCTCTA
XM_017000143.1:c.671+447_671+451delinsCTCTA	XP_016855632.1:n.671+447_671+451delinsCTCTA
XM_017000144.1:c.443+447_443+451delinsCTCTA	XP_016855633.1:n.443+447_443+451delinsCTCTA
XR_002959248.1:n.1677+568_1677+572delinsCTCTA
XR_002959249.1:n.1309+568_1309+572delinsCTCTA
NM_053274.3:c.1214+447_1214+451delinsCTCTA MANE Select	NP_444504.1:n.1214+447_1214+451delinsCTCTA
NM_001319683.2:c.1172+447_1172+451delinsCTCTA	NP_001306612.1:n.1172+447_1172+451delinsCTCTA
NR_135089.2:n.1307+447_1307+451delinsCTCTA