Canonical Allele Identifier: CA341099531

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92731980A>C (hg19) ; chr1:g.92266423A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266423A>C , CM000663.2:g.92266423A>C	GRCh38
NC_000001.10:g.92731980A>C , CM000663.1:g.92731980A>C	GRCh37
NC_000001.9:g.92504568A>C	NCBI36
NG_009796.1:g.37587T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1210T>G MANE Select	ENSP00000359385.3:p.Phe404Val
ENST00000370360.7:c.1210T>G	ENSP00000359385.3:p.Phe404Val
ENST00000463560.1:c.562+117T>G
ENST00000495106.5:c.1210T>G	ENSP00000436829.1:p.Phe404Val
ENST00000495852.6:c.433T>G	ENSP00000469157.2:p.Phe145Val
NM_053274.2:c.1210T>G	NP_444504.1:p.Phe404Val
XM_005270400.1:c.1168T>G	XP_005270457.1:p.Phe390Val
XM_005270401.2:c.1084T>G	XP_005270458.1:p.Phe362Val
XM_006710309.1:c.709T>G	XP_006710372.1:p.Phe237Val
XM_011540544.1:c.1210T>G	XP_011538846.1:p.Phe404Val
XM_011540545.1:c.1210T>G	XP_011538847.1:p.Phe404Val
XM_011540546.1:c.1210T>G	XP_011538848.1:p.Phe404Val
XR_946529.1:n.1309+117T>G
NM_001319683.1:c.1168T>G	NP_001306612.1:p.Phe390Val
NR_135089.1:n.1325T>G
XM_005270401.3:c.1084T>G	XP_005270458.1:p.Phe362Val
XM_006710309.2:c.709T>G	XP_006710372.1:p.Phe237Val
XM_011540546.2:c.1210T>G	XP_011538848.1:p.Phe404Val
XM_017000137.1:c.1309T>G	XP_016855626.1:p.Phe437Val
XM_017000138.1:c.1267T>G	XP_016855627.1:p.Phe423Val
XM_017000139.1:c.1293+117T>G	XP_016855628.1:n.1293+117T>G
XM_017000140.1:c.1183T>G	XP_016855629.1:p.Phe395Val
XM_017000141.1:c.1194+117T>G	XP_016855630.1:n.1194+117T>G
XM_017000142.1:c.667T>G	XP_016855631.1:p.Phe223Val
XM_017000143.1:c.667T>G	XP_016855632.1:p.Phe223Val
XM_017000144.1:c.439T>G	XP_016855633.1:p.Phe147Val
XR_002959248.1:n.1677+117T>G
XR_002959249.1:n.1309+117T>G
NM_053274.3:c.1210T>G MANE Select	NP_444504.1:p.Phe404Val
NM_001319683.2:c.1168T>G	NP_001306612.1:p.Phe390Val
NR_135089.2:n.1303T>G