Canonical Allele Identifier: CA950589

Gene: GLMN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92289110C>T , CM000663.2:g.92289110C>T	GRCh38
NC_000001.10:g.92754667C>T , CM000663.1:g.92754667C>T	GRCh37
NC_000001.9:g.92527255C>T	NCBI36
NG_009796.1:g.14900G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.436G>A MANE Select	ENSP00000359385.3:p.Ala146Thr
ENST00000370360.7:c.436G>A	ENSP00000359385.3:p.Ala146Thr
ENST00000495106.5:c.436G>A	ENSP00000436829.1:p.Ala146Thr
NM_053274.2:c.436G>A	NP_444504.1:p.Ala146Thr
XM_005270400.1:c.436G>A	XP_005270457.1:p.Ala146Thr
XM_005270401.2:c.310G>A	XP_005270458.1:p.Ala104Thr
XM_006710309.1:c.-66G>A	XP_006710372.1:n.-66G>A
XM_011540544.1:c.436G>A	XP_011538846.1:p.Ala146Thr
XM_011540545.1:c.436G>A	XP_011538847.1:p.Ala146Thr
XM_011540546.1:c.436G>A	XP_011538848.1:p.Ala146Thr
XR_946529.1:n.551G>A
NM_001319683.1:c.436G>A	NP_001306612.1:p.Ala146Thr
NR_135089.1:n.551G>A
XM_005270401.3:c.310G>A	XP_005270458.1:p.Ala104Thr
XM_006710309.2:c.-66G>A	XP_006710372.1:n.-66G>A
XM_011540546.2:c.436G>A	XP_011538848.1:p.Ala146Thr
XM_017000137.1:c.535G>A	XP_016855626.1:p.Ala179Thr
XM_017000138.1:c.535G>A	XP_016855627.1:p.Ala179Thr
XM_017000139.1:c.535G>A	XP_016855628.1:p.Ala179Thr
XM_017000140.1:c.409G>A	XP_016855629.1:p.Ala137Thr
XM_017000141.1:c.436G>A	XP_016855630.1:p.Ala146Thr
XM_017000142.1:c.-66G>A	XP_016855631.1:n.-66G>A
XM_017000143.1:c.-66G>A	XP_016855632.1:n.-66G>A
XM_017000144.1:c.-233G>A	XP_016855633.1:n.-233G>A
XR_002959248.1:n.919G>A
XR_002959249.1:n.551G>A
NM_053274.3:c.436G>A MANE Select	NP_444504.1:p.Ala146Thr
NM_001319683.2:c.436G>A	NP_001306612.1:p.Ala146Thr
NR_135089.2:n.529G>A