Canonical Allele Identifier: CA418785861

Gene: GLMN

Linked Data

• MyVariant Identifiers: chr1:g.92732008C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92266451C>T , CM000663.2:g.92266451C>T	GRCh38
NC_000001.10:g.92732008C>T , CM000663.1:g.92732008C>T	GRCh37
NC_000001.9:g.92504596C>T	NCBI36
NG_009796.1:g.37559G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370360.8:c.1182G>A MANE Select	ENSP00000359385.3:p.Lys394=
ENST00000370360.7:c.1182G>A	ENSP00000359385.3:p.Lys394=
ENST00000463560.1:c.562+89G>A
ENST00000495106.5:c.1182G>A	ENSP00000436829.1:p.Lys394=
ENST00000495852.6:c.405G>A	ENSP00000469157.2:p.Lys135=
NM_053274.2:c.1182G>A	NP_444504.1:p.Lys394=
XM_005270400.1:c.1140G>A	XP_005270457.1:p.Lys380=
XM_005270401.2:c.1056G>A	XP_005270458.1:p.Lys352=
XM_006710309.1:c.681G>A	XP_006710372.1:p.Lys227=
XM_011540544.1:c.1182G>A	XP_011538846.1:p.Lys394=
XM_011540545.1:c.1182G>A	XP_011538847.1:p.Lys394=
XM_011540546.1:c.1182G>A	XP_011538848.1:p.Lys394=
XR_946529.1:n.1309+89G>A
NM_001319683.1:c.1140G>A	NP_001306612.1:p.Lys380=
NR_135089.1:n.1297G>A
XM_005270401.3:c.1056G>A	XP_005270458.1:p.Lys352=
XM_006710309.2:c.681G>A	XP_006710372.1:p.Lys227=
XM_011540546.2:c.1182G>A	XP_011538848.1:p.Lys394=
XM_017000137.1:c.1281G>A	XP_016855626.1:p.Lys427=
XM_017000138.1:c.1239G>A	XP_016855627.1:p.Lys413=
XM_017000139.1:c.1293+89G>A	XP_016855628.1:n.1293+89G>A
XM_017000140.1:c.1155G>A	XP_016855629.1:p.Lys385=
XM_017000141.1:c.1194+89G>A	XP_016855630.1:n.1194+89G>A
XM_017000142.1:c.639G>A	XP_016855631.1:p.Lys213=
XM_017000143.1:c.639G>A	XP_016855632.1:p.Lys213=
XM_017000144.1:c.411G>A	XP_016855633.1:p.Lys137=
XR_002959248.1:n.1677+89G>A
XR_002959249.1:n.1309+89G>A
NM_053274.3:c.1182G>A MANE Select	NP_444504.1:p.Lys394=
NM_001319683.2:c.1140G>A	NP_001306612.1:p.Lys380=
NR_135089.2:n.1275G>A