Canonical Allele Identifier: CA950351
Gene: GLMN HGNC NCBI

Linked Data

dbSNP Id: rs754711361
gnomAD v2: 1-92732150-C-T
gnomAD v4: 1-92266593-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92266593C>T , CM000663.2:g.92266593C>T GRCh38
NC_000001.10:g.92732150C>T , CM000663.1:g.92732150C>T GRCh37
NC_000001.9:g.92504738C>T NCBI36
NG_009796.1:g.37417G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370360.8:c.1141-101G>A MANE Select ENSP00000359385.3:n.1141-101G>A
ENST00000370360.7:c.1141-101G>A ENSP00000359385.3:n.1141-101G>A
ENST00000463560.1:c.509G>A
ENST00000495106.5:c.1141-101G>A ENSP00000436829.1:n.1141-101G>A
ENST00000495852.6:c.364-101G>A ENSP00000469157.2:n.364-101G>A
NM_053274.2:c.1141-101G>A NP_444504.1:n.1141-101G>A
XM_005270400.1:c.1099-101G>A XP_005270457.1:n.1099-101G>A
XM_005270401.2:c.1015-101G>A XP_005270458.1:n.1015-101G>A
XM_006710309.1:c.640-101G>A XP_006710372.1:n.640-101G>A
XM_011540544.1:c.1141-101G>A XP_011538846.1:n.1141-101G>A
XM_011540545.1:c.1141-101G>A XP_011538847.1:n.1141-101G>A
XM_011540546.1:c.1141-101G>A XP_011538848.1:n.1141-101G>A
XR_946529.1:n.1256G>A
NM_001319683.1:c.1099-101G>A NP_001306612.1:n.1099-101G>A
NR_135089.1:n.1256-101G>A
XM_005270401.3:c.1015-101G>A XP_005270458.1:n.1015-101G>A
XM_006710309.2:c.640-101G>A XP_006710372.1:n.640-101G>A
XM_011540546.2:c.1141-101G>A XP_011538848.1:n.1141-101G>A
XM_017000137.1:c.1240-101G>A XP_016855626.1:n.1240-101G>A
XM_017000138.1:c.1198-101G>A XP_016855627.1:n.1198-101G>A
XM_017000139.1:c.1240G>A XP_016855628.1:p.Glu414Lys
XM_017000140.1:c.1114-101G>A XP_016855629.1:n.1114-101G>A
XM_017000141.1:c.1141G>A XP_016855630.1:p.Glu381Lys
XM_017000142.1:c.598-101G>A XP_016855631.1:n.598-101G>A
XM_017000143.1:c.598-101G>A XP_016855632.1:n.598-101G>A
XM_017000144.1:c.370-101G>A XP_016855633.1:n.370-101G>A
XR_002959248.1:n.1624G>A
XR_002959249.1:n.1256G>A
NM_053274.3:c.1141-101G>A MANE Select NP_444504.1:n.1141-101G>A
NM_001319683.2:c.1099-101G>A NP_001306612.1:n.1099-101G>A
NR_135089.2:n.1234-101G>A