Canonical Allele Identifier: CA26733025

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92246595G>A , CM000663.2:g.92246595G>A	GRCh38
NC_000001.10:g.92712152G>A , CM000663.1:g.92712152G>A	GRCh37
NC_000001.9:g.92484740G>A	NCBI36
NG_009796.1:g.57415C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1720C>T MANE Select	ENSP00000359385.3:p.Arg574Ter
ENST00000370360.7:c.1720C>T	ENSP00000359385.3:p.Arg574Ter
ENST00000471465.1:n.666C>T
ENST00000495106.5:c.*381C>T	ENSP00000436829.1:n.*381C>T
NM_053274.2:c.1720C>T	NP_444504.1:p.Arg574Ter
XM_005270400.1:c.1678C>T	XP_005270457.1:p.Arg560Ter
XM_005270401.2:c.1594C>T	XP_005270458.1:p.Arg532Ter
XM_006710309.1:c.1219C>T	XP_006710372.1:p.Arg407Ter
XM_011540544.1:c.1720C>T	XP_011538846.1:p.Arg574Ter
XM_011540545.1:c.1720C>T	XP_011538847.1:p.Arg574Ter
XM_011540546.1:c.1720C>T	XP_011538848.1:p.Arg574Ter
NM_001319683.1:c.1678C>T	NP_001306612.1:p.Arg560Ter
NR_135089.1:n.1750C>T
XM_005270401.3:c.1594C>T	XP_005270458.1:p.Arg532Ter
XM_006710309.2:c.1219C>T	XP_006710372.1:p.Arg407Ter
XM_011540546.2:c.1720C>T	XP_011538848.1:p.Arg574Ter
XM_017000137.1:c.1819C>T	XP_016855626.1:p.Arg607Ter
XM_017000138.1:c.1777C>T	XP_016855627.1:p.Arg593Ter
XM_017000139.1:c.1714C>T	XP_016855628.1:p.Arg572Ter
XM_017000140.1:c.1693C>T	XP_016855629.1:p.Arg565Ter
XM_017000141.1:c.1615C>T	XP_016855630.1:p.Arg539Ter
XM_017000142.1:c.1177C>T	XP_016855631.1:p.Arg393Ter
XM_017000143.1:c.1177C>T	XP_016855632.1:p.Arg393Ter
XM_017000144.1:c.949C>T	XP_016855633.1:p.Arg317Ter
XR_002959248.1:n.2183C>T
XR_002959249.1:n.1815C>T
NM_053274.3:c.1720C>T MANE Select	NP_444504.1:p.Arg574Ter
NM_001319683.2:c.1678C>T	NP_001306612.1:p.Arg560Ter
NR_135089.2:n.1728C>T