Canonical Allele Identifier: CA341099627

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92732002A>C (hg19) ; chr1:g.92266445A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266445A>C , CM000663.2:g.92266445A>C	GRCh38
NC_000001.10:g.92732002A>C , CM000663.1:g.92732002A>C	GRCh37
NC_000001.9:g.92504590A>C	NCBI36
NG_009796.1:g.37565T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1188T>G MANE Select	ENSP00000359385.3:p.Asp396Glu
ENST00000370360.7:c.1188T>G	ENSP00000359385.3:p.Asp396Glu
ENST00000463560.1:c.562+95T>G
ENST00000495106.5:c.1188T>G	ENSP00000436829.1:p.Asp396Glu
ENST00000495852.6:c.411T>G	ENSP00000469157.2:p.Asp137Glu
NM_053274.2:c.1188T>G	NP_444504.1:p.Asp396Glu
XM_005270400.1:c.1146T>G	XP_005270457.1:p.Asp382Glu
XM_005270401.2:c.1062T>G	XP_005270458.1:p.Asp354Glu
XM_006710309.1:c.687T>G	XP_006710372.1:p.Asp229Glu
XM_011540544.1:c.1188T>G	XP_011538846.1:p.Asp396Glu
XM_011540545.1:c.1188T>G	XP_011538847.1:p.Asp396Glu
XM_011540546.1:c.1188T>G	XP_011538848.1:p.Asp396Glu
XR_946529.1:n.1309+95T>G
NM_001319683.1:c.1146T>G	NP_001306612.1:p.Asp382Glu
NR_135089.1:n.1303T>G
XM_005270401.3:c.1062T>G	XP_005270458.1:p.Asp354Glu
XM_006710309.2:c.687T>G	XP_006710372.1:p.Asp229Glu
XM_011540546.2:c.1188T>G	XP_011538848.1:p.Asp396Glu
XM_017000137.1:c.1287T>G	XP_016855626.1:p.Asp429Glu
XM_017000138.1:c.1245T>G	XP_016855627.1:p.Asp415Glu
XM_017000139.1:c.1293+95T>G	XP_016855628.1:n.1293+95T>G
XM_017000140.1:c.1161T>G	XP_016855629.1:p.Asp387Glu
XM_017000141.1:c.1194+95T>G	XP_016855630.1:n.1194+95T>G
XM_017000142.1:c.645T>G	XP_016855631.1:p.Asp215Glu
XM_017000143.1:c.645T>G	XP_016855632.1:p.Asp215Glu
XM_017000144.1:c.417T>G	XP_016855633.1:p.Asp139Glu
XR_002959248.1:n.1677+95T>G
XR_002959249.1:n.1309+95T>G
NM_053274.3:c.1188T>G MANE Select	NP_444504.1:p.Asp396Glu
NM_001319683.2:c.1146T>G	NP_001306612.1:p.Asp382Glu
NR_135089.2:n.1281T>G