Canonical Allele Identifier: CA341099594

Gene: GLMN

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1195G>C MANE Select	ENSP00000359385.3:p.Gly399Arg
ENST00000370360.7:c.1195G>C	ENSP00000359385.3:p.Gly399Arg
ENST00000463560.1:c.562+102G>C
ENST00000495106.5:c.1195G>C	ENSP00000436829.1:p.Gly399Arg
ENST00000495852.6:c.418G>C	ENSP00000469157.2:p.Gly140Arg
NM_053274.2:c.1195G>C	NP_444504.1:p.Gly399Arg
XM_005270400.1:c.1153G>C	XP_005270457.1:p.Gly385Arg
XM_005270401.2:c.1069G>C	XP_005270458.1:p.Gly357Arg
XM_006710309.1:c.694G>C	XP_006710372.1:p.Gly232Arg
XM_011540544.1:c.1195G>C	XP_011538846.1:p.Gly399Arg
XM_011540545.1:c.1195G>C	XP_011538847.1:p.Gly399Arg
XM_011540546.1:c.1195G>C	XP_011538848.1:p.Gly399Arg
XR_946529.1:n.1309+102G>C
NM_001319683.1:c.1153G>C	NP_001306612.1:p.Gly385Arg
NR_135089.1:n.1310G>C
XM_005270401.3:c.1069G>C	XP_005270458.1:p.Gly357Arg
XM_006710309.2:c.694G>C	XP_006710372.1:p.Gly232Arg
XM_011540546.2:c.1195G>C	XP_011538848.1:p.Gly399Arg
XM_017000137.1:c.1294G>C	XP_016855626.1:p.Gly432Arg
XM_017000138.1:c.1252G>C	XP_016855627.1:p.Gly418Arg
XM_017000139.1:c.1293+102G>C	XP_016855628.1:n.1293+102G>C
XM_017000140.1:c.1168G>C	XP_016855629.1:p.Gly390Arg
XM_017000141.1:c.1194+102G>C	XP_016855630.1:n.1194+102G>C
XM_017000142.1:c.652G>C	XP_016855631.1:p.Gly218Arg
XM_017000143.1:c.652G>C	XP_016855632.1:p.Gly218Arg
XM_017000144.1:c.424G>C	XP_016855633.1:p.Gly142Arg
XR_002959248.1:n.1677+102G>C
XR_002959249.1:n.1309+102G>C
NM_053274.3:c.1195G>C MANE Select	NP_444504.1:p.Gly399Arg
NM_001319683.2:c.1153G>C	NP_001306612.1:p.Gly385Arg
NR_135089.2:n.1288G>C