Canonical Allele Identifier: CA26744758

Gene: GLMN

Linked Data

• dbSNP Id: rs919382169
• gnomAD v3: 1-92265958-A-ATCTT
• gnomAD v4: 1-92265958-A-ATCTT
• MyVariant Identifiers: chr1:g.92731515_92731516insTCTT (hg19) ; chr1:g.92265958_92265959insTCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92265960_92265963dup , CM000663.2:g.92265960_92265963dup	GRCh38
NC_000001.10:g.92731517_92731520dup , CM000663.1:g.92731517_92731520dup	GRCh37
NC_000001.9:g.92504105_92504108dup	NCBI36
NG_009796.1:g.38048_38051dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1214+457_1214+460dup MANE Select	ENSP00000359385.3:n.1214+457_1214+460dup
ENST00000370360.7:c.1214+457_1214+460dup	ENSP00000359385.3:n.1214+457_1214+460dup
ENST00000463560.1:c.562+578_562+581dup
ENST00000495106.5:c.1214+457_1214+460dup	ENSP00000436829.1:n.1214+457_1214+460dup
ENST00000495852.6:c.437+457_437+460dup	ENSP00000469157.2:n.437+457_437+460dup
NM_053274.2:c.1214+457_1214+460dup	NP_444504.1:n.1214+457_1214+460dup
XM_005270400.1:c.1172+457_1172+460dup	XP_005270457.1:n.1172+457_1172+460dup
XM_005270401.2:c.1088+457_1088+460dup	XP_005270458.1:n.1088+457_1088+460dup
XM_006710309.1:c.713+457_713+460dup	XP_006710372.1:n.713+457_713+460dup
XM_011540544.1:c.1214+457_1214+460dup	XP_011538846.1:n.1214+457_1214+460dup
XM_011540545.1:c.1214+457_1214+460dup	XP_011538847.1:n.1214+457_1214+460dup
XM_011540546.1:c.1214+457_1214+460dup	XP_011538848.1:n.1214+457_1214+460dup
XR_946529.1:n.1309+578_1309+581dup
NM_001319683.1:c.1172+457_1172+460dup	NP_001306612.1:n.1172+457_1172+460dup
NR_135089.1:n.1329+457_1329+460dup
XM_005270401.3:c.1088+457_1088+460dup	XP_005270458.1:n.1088+457_1088+460dup
XM_006710309.2:c.713+457_713+460dup	XP_006710372.1:n.713+457_713+460dup
XM_011540546.2:c.1214+457_1214+460dup	XP_011538848.1:n.1214+457_1214+460dup
XM_017000137.1:c.1313+457_1313+460dup	XP_016855626.1:n.1313+457_1313+460dup
XM_017000138.1:c.1271+457_1271+460dup	XP_016855627.1:n.1271+457_1271+460dup
XM_017000139.1:c.1293+578_1293+581dup	XP_016855628.1:n.1293+578_1293+581dup
XM_017000140.1:c.1187+457_1187+460dup	XP_016855629.1:n.1187+457_1187+460dup
XM_017000141.1:c.1194+578_1194+581dup	XP_016855630.1:n.1194+578_1194+581dup
XM_017000142.1:c.671+457_671+460dup	XP_016855631.1:n.671+457_671+460dup
XM_017000143.1:c.671+457_671+460dup	XP_016855632.1:n.671+457_671+460dup
XM_017000144.1:c.443+457_443+460dup	XP_016855633.1:n.443+457_443+460dup
XR_002959248.1:n.1677+578_1677+581dup
XR_002959249.1:n.1309+578_1309+581dup
NM_053274.3:c.1214+457_1214+460dup MANE Select	NP_444504.1:n.1214+457_1214+460dup
NM_001319683.2:c.1172+457_1172+460dup	NP_001306612.1:n.1172+457_1172+460dup
NR_135089.2:n.1307+457_1307+460dup