Canonical Allele Identifier: CA341099562

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92731988T>A (hg19) ; chr1:g.92266431T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266431T>A , CM000663.2:g.92266431T>A	GRCh38
NC_000001.10:g.92731988T>A , CM000663.1:g.92731988T>A	GRCh37
NC_000001.9:g.92504576T>A	NCBI36
NG_009796.1:g.37579A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370360.8:c.1202A>T MANE Select	ENSP00000359385.3:p.Tyr401Phe
ENST00000370360.7:c.1202A>T	ENSP00000359385.3:p.Tyr401Phe
ENST00000463560.1:c.562+109A>T
ENST00000495106.5:c.1202A>T	ENSP00000436829.1:p.Tyr401Phe
ENST00000495852.6:c.425A>T	ENSP00000469157.2:p.Tyr142Phe
NM_053274.2:c.1202A>T	NP_444504.1:p.Tyr401Phe
XM_005270400.1:c.1160A>T	XP_005270457.1:p.Tyr387Phe
XM_005270401.2:c.1076A>T	XP_005270458.1:p.Tyr359Phe
XM_006710309.1:c.701A>T	XP_006710372.1:p.Tyr234Phe
XM_011540544.1:c.1202A>T	XP_011538846.1:p.Tyr401Phe
XM_011540545.1:c.1202A>T	XP_011538847.1:p.Tyr401Phe
XM_011540546.1:c.1202A>T	XP_011538848.1:p.Tyr401Phe
XR_946529.1:n.1309+109A>T
NM_001319683.1:c.1160A>T	NP_001306612.1:p.Tyr387Phe
NR_135089.1:n.1317A>T
XM_005270401.3:c.1076A>T	XP_005270458.1:p.Tyr359Phe
XM_006710309.2:c.701A>T	XP_006710372.1:p.Tyr234Phe
XM_011540546.2:c.1202A>T	XP_011538848.1:p.Tyr401Phe
XM_017000137.1:c.1301A>T	XP_016855626.1:p.Tyr434Phe
XM_017000138.1:c.1259A>T	XP_016855627.1:p.Tyr420Phe
XM_017000139.1:c.1293+109A>T	XP_016855628.1:n.1293+109A>T
XM_017000140.1:c.1175A>T	XP_016855629.1:p.Tyr392Phe
XM_017000141.1:c.1194+109A>T	XP_016855630.1:n.1194+109A>T
XM_017000142.1:c.659A>T	XP_016855631.1:p.Tyr220Phe
XM_017000143.1:c.659A>T	XP_016855632.1:p.Tyr220Phe
XM_017000144.1:c.431A>T	XP_016855633.1:p.Tyr144Phe
XR_002959248.1:n.1677+109A>T
XR_002959249.1:n.1309+109A>T
NM_053274.3:c.1202A>T MANE Select	NP_444504.1:p.Tyr401Phe
NM_001319683.2:c.1160A>T	NP_001306612.1:p.Tyr387Phe
NR_135089.2:n.1295A>T