Canonical Allele Identifier: CA375046325

Gene: GLE1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1106T>G	ENSP00000507095.1:n.*1106T>G
ENST00000683288.1:c.*2034T>G	ENSP00000507477.1:n.*2034T>G
ENST00000683748.1:c.2062T>G	ENSP00000507377.1:p.Leu688Val
ENST00000683905.1:c.*711T>G	ENSP00000506960.1:n.*711T>G
ENST00000684139.1:c.1570T>G	ENSP00000507295.1:p.Leu524Val
ENST00000684210.1:n.1748T>G
ENST00000684314.1:c.1930T>G	ENSP00000507700.1:p.Leu644Val
ENST00000684331.1:c.*755T>G	ENSP00000507431.1:n.*755T>G
ENST00000684463.1:n.673T>G
ENST00000684646.1:c.1822T>G	ENSP00000507723.1:p.Leu608Val
ENST00000309971.9:c.2035T>G MANE Select	ENSP00000308622.5:p.Leu679Val
ENST00000309971.8:c.2035T>G	ENSP00000308622.4:p.Leu679Val
NM_001003722.1:c.2035T>G , LRG_484t1:c.2035T>G	NP_001003722.1:p.Leu679Val
XM_006717059.2:c.2071T>G	XP_006717122.1:p.Leu691Val
XM_006717060.2:c.2044T>G	XP_006717123.1:p.Leu682Val
XM_011518549.1:c.2071T>G	XP_011516851.1:p.Leu691Val
XM_011518550.1:c.2071T>G	XP_011516852.1:p.Leu691Val
XM_011518551.1:c.2062T>G	XP_011516853.1:p.Leu688Val
XM_011518552.1:c.1312T>G	XP_011516854.1:p.Leu438Val
XR_242681.3:n.100+2271A>C
XM_006717059.3:c.2071T>G	XP_006717122.1:p.Leu691Val
XM_006717060.3:c.2044T>G	XP_006717123.1:p.Leu682Val
XM_011518551.2:c.2062T>G	XP_011516853.1:p.Leu688Val
XM_024447519.1:c.2044T>G	XP_024303287.1:p.Leu682Val
NM_001003722.2:c.2035T>G MANE Select	NP_001003722.1:p.Leu679Val