Canonical Allele Identifier: CA375046324

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131303387T>A (hg19) ; chr9:g.128541108T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541108T>A , CM000671.2:g.128541108T>A	GRCh38
NC_000009.11:g.131303387T>A , CM000671.1:g.131303387T>A	GRCh37
NC_000009.10:g.130343208T>A	NCBI36
NG_012073.1:g.41417T>A , LRG_484:g.41417T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1106T>A	ENSP00000507095.1:n.*1106T>A
ENST00000683288.1:c.*2034T>A	ENSP00000507477.1:n.*2034T>A
ENST00000683748.1:c.2062T>A	ENSP00000507377.1:p.Leu688Met
ENST00000683905.1:c.*711T>A	ENSP00000506960.1:n.*711T>A
ENST00000684139.1:c.1570T>A	ENSP00000507295.1:p.Leu524Met
ENST00000684210.1:n.1748T>A
ENST00000684314.1:c.1930T>A	ENSP00000507700.1:p.Leu644Met
ENST00000684331.1:c.*755T>A	ENSP00000507431.1:n.*755T>A
ENST00000684463.1:n.673T>A
ENST00000684646.1:c.1822T>A	ENSP00000507723.1:p.Leu608Met
ENST00000309971.9:c.2035T>A MANE Select	ENSP00000308622.5:p.Leu679Met
ENST00000309971.8:c.2035T>A	ENSP00000308622.4:p.Leu679Met
NM_001003722.1:c.2035T>A , LRG_484t1:c.2035T>A	NP_001003722.1:p.Leu679Met
XM_006717059.2:c.2071T>A	XP_006717122.1:p.Leu691Met
XM_006717060.2:c.2044T>A	XP_006717123.1:p.Leu682Met
XM_011518549.1:c.2071T>A	XP_011516851.1:p.Leu691Met
XM_011518550.1:c.2071T>A	XP_011516852.1:p.Leu691Met
XM_011518551.1:c.2062T>A	XP_011516853.1:p.Leu688Met
XM_011518552.1:c.1312T>A	XP_011516854.1:p.Leu438Met
XR_242681.3:n.100+2271A>T
XM_006717059.3:c.2071T>A	XP_006717122.1:p.Leu691Met
XM_006717060.3:c.2044T>A	XP_006717123.1:p.Leu682Met
XM_011518551.2:c.2062T>A	XP_011516853.1:p.Leu688Met
XM_024447519.1:c.2044T>A	XP_024303287.1:p.Leu682Met
NM_001003722.2:c.2035T>A MANE Select	NP_001003722.1:p.Leu679Met