Canonical Allele Identifier: CA341099592

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92731995C>A (hg19) ; chr1:g.92266438C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266438C>A , CM000663.2:g.92266438C>A	GRCh38
NC_000001.10:g.92731995C>A , CM000663.1:g.92731995C>A	GRCh37
NC_000001.9:g.92504583C>A	NCBI36
NG_009796.1:g.37572G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1195G>T MANE Select	ENSP00000359385.3:p.Gly399Cys
ENST00000370360.7:c.1195G>T	ENSP00000359385.3:p.Gly399Cys
ENST00000463560.1:c.562+102G>T
ENST00000495106.5:c.1195G>T	ENSP00000436829.1:p.Gly399Cys
ENST00000495852.6:c.418G>T	ENSP00000469157.2:p.Gly140Cys
NM_053274.2:c.1195G>T	NP_444504.1:p.Gly399Cys
XM_005270400.1:c.1153G>T	XP_005270457.1:p.Gly385Cys
XM_005270401.2:c.1069G>T	XP_005270458.1:p.Gly357Cys
XM_006710309.1:c.694G>T	XP_006710372.1:p.Gly232Cys
XM_011540544.1:c.1195G>T	XP_011538846.1:p.Gly399Cys
XM_011540545.1:c.1195G>T	XP_011538847.1:p.Gly399Cys
XM_011540546.1:c.1195G>T	XP_011538848.1:p.Gly399Cys
XR_946529.1:n.1309+102G>T
NM_001319683.1:c.1153G>T	NP_001306612.1:p.Gly385Cys
NR_135089.1:n.1310G>T
XM_005270401.3:c.1069G>T	XP_005270458.1:p.Gly357Cys
XM_006710309.2:c.694G>T	XP_006710372.1:p.Gly232Cys
XM_011540546.2:c.1195G>T	XP_011538848.1:p.Gly399Cys
XM_017000137.1:c.1294G>T	XP_016855626.1:p.Gly432Cys
XM_017000138.1:c.1252G>T	XP_016855627.1:p.Gly418Cys
XM_017000139.1:c.1293+102G>T	XP_016855628.1:n.1293+102G>T
XM_017000140.1:c.1168G>T	XP_016855629.1:p.Gly390Cys
XM_017000141.1:c.1194+102G>T	XP_016855630.1:n.1194+102G>T
XM_017000142.1:c.652G>T	XP_016855631.1:p.Gly218Cys
XM_017000143.1:c.652G>T	XP_016855632.1:p.Gly218Cys
XM_017000144.1:c.424G>T	XP_016855633.1:p.Gly142Cys
XR_002959248.1:n.1677+102G>T
XR_002959249.1:n.1309+102G>T
NM_053274.3:c.1195G>T MANE Select	NP_444504.1:p.Gly399Cys
NM_001319683.2:c.1153G>T	NP_001306612.1:p.Gly385Cys
NR_135089.2:n.1288G>T