Canonical Allele Identifier: CA341099528

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92731979A>C (hg19) ; chr1:g.92266422A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266422A>C , CM000663.2:g.92266422A>C	GRCh38
NC_000001.10:g.92731979A>C , CM000663.1:g.92731979A>C	GRCh37
NC_000001.9:g.92504567A>C	NCBI36
NG_009796.1:g.37588T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1211T>G MANE Select	ENSP00000359385.3:p.Phe404Cys
ENST00000370360.7:c.1211T>G	ENSP00000359385.3:p.Phe404Cys
ENST00000463560.1:c.562+118T>G
ENST00000495106.5:c.1211T>G	ENSP00000436829.1:p.Phe404Cys
ENST00000495852.6:c.434T>G	ENSP00000469157.2:p.Phe145Cys
NM_053274.2:c.1211T>G	NP_444504.1:p.Phe404Cys
XM_005270400.1:c.1169T>G	XP_005270457.1:p.Phe390Cys
XM_005270401.2:c.1085T>G	XP_005270458.1:p.Phe362Cys
XM_006710309.1:c.710T>G	XP_006710372.1:p.Phe237Cys
XM_011540544.1:c.1211T>G	XP_011538846.1:p.Phe404Cys
XM_011540545.1:c.1211T>G	XP_011538847.1:p.Phe404Cys
XM_011540546.1:c.1211T>G	XP_011538848.1:p.Phe404Cys
XR_946529.1:n.1309+118T>G
NM_001319683.1:c.1169T>G	NP_001306612.1:p.Phe390Cys
NR_135089.1:n.1326T>G
XM_005270401.3:c.1085T>G	XP_005270458.1:p.Phe362Cys
XM_006710309.2:c.710T>G	XP_006710372.1:p.Phe237Cys
XM_011540546.2:c.1211T>G	XP_011538848.1:p.Phe404Cys
XM_017000137.1:c.1310T>G	XP_016855626.1:p.Phe437Cys
XM_017000138.1:c.1268T>G	XP_016855627.1:p.Phe423Cys
XM_017000139.1:c.1293+118T>G	XP_016855628.1:n.1293+118T>G
XM_017000140.1:c.1184T>G	XP_016855629.1:p.Phe395Cys
XM_017000141.1:c.1194+118T>G	XP_016855630.1:n.1194+118T>G
XM_017000142.1:c.668T>G	XP_016855631.1:p.Phe223Cys
XM_017000143.1:c.668T>G	XP_016855632.1:p.Phe223Cys
XM_017000144.1:c.440T>G	XP_016855633.1:p.Phe147Cys
XR_002959248.1:n.1677+118T>G
XR_002959249.1:n.1309+118T>G
NM_053274.3:c.1211T>G MANE Select	NP_444504.1:p.Phe404Cys
NM_001319683.2:c.1169T>G	NP_001306612.1:p.Phe390Cys
NR_135089.2:n.1304T>G