Canonical Allele Identifier: CA1880332305

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540316T= , CM000671.2:g.128540316T=	GRCh38
NC_000009.11:g.131302595T= , CM000671.1:g.131302595T=	GRCh37
NC_000009.10:g.130342416T=	NCBI36
NG_012073.1:g.40625T= , LRG_484:g.40625T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1077T=	ENSP00000507095.1:n.*1077T=
ENST00000683288.1:c.*2005T=	ENSP00000507477.1:n.*2005T=
ENST00000683748.1:c.2033T=	ENSP00000507377.1:p.Ile678=
ENST00000683905.1:c.*682T=	ENSP00000506960.1:n.*682T=
ENST00000684139.1:c.1541T=	ENSP00000507295.1:p.Ile514=
ENST00000684210.1:n.1719T=
ENST00000684314.1:c.1901T=	ENSP00000507700.1:p.Ile634=
ENST00000684331.1:c.2006T=	ENSP00000507431.1:p.Ile669=
ENST00000684463.1:n.644T=
ENST00000684646.1:c.1793T=	ENSP00000507723.1:p.Ile598=
ENST00000309971.9:c.2006T= MANE Select	ENSP00000308622.5:p.Ile669=
ENST00000309971.8:c.2006T=	ENSP00000308622.4:p.Ile669=
NM_001003722.1:c.2006T= , LRG_484t1:c.2006T=	NP_001003722.1:p.Ile669=
XM_006717059.2:c.2042T=	XP_006717122.1:p.Ile681=
XM_006717060.2:c.2015T=	XP_006717123.1:p.Ile672=
XM_011518549.1:c.2042T=	XP_011516851.1:p.Ile681=
XM_011518550.1:c.2042T=	XP_011516852.1:p.Ile681=
XM_011518551.1:c.2033T=	XP_011516853.1:p.Ile678=
XM_011518552.1:c.1283T=	XP_011516854.1:p.Ile428=
XR_242681.3:n.100+3063A=
XR_428600.2:n.124+654A=
XM_006717059.3:c.2042T=	XP_006717122.1:p.Ile681=
XM_006717060.3:c.2015T=	XP_006717123.1:p.Ile672=
XM_011518551.2:c.2033T=	XP_011516853.1:p.Ile678=
XM_024447519.1:c.2015T=	XP_024303287.1:p.Ile672=
XR_428600.3:n.126+654A=
NM_001003722.2:c.2006T= MANE Select	NP_001003722.1:p.Ile669=