Canonical Allele Identifier: CA1880332308

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540317A= , CM000671.2:g.128540317A=	GRCh38
NC_000009.11:g.131302596A= , CM000671.1:g.131302596A=	GRCh37
NC_000009.10:g.130342417A=	NCBI36
NG_012073.1:g.40626A= , LRG_484:g.40626A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000683044.1:c.*1078A=	ENSP00000507095.1:n.*1078A=
ENST00000683288.1:c.*2006A=	ENSP00000507477.1:n.*2006A=
ENST00000683748.1:c.2034A=	ENSP00000507377.1:p.Ile678=
ENST00000683905.1:c.*683A=	ENSP00000506960.1:n.*683A=
ENST00000684139.1:c.1542A=	ENSP00000507295.1:p.Ile514=
ENST00000684210.1:n.1720A=
ENST00000684314.1:c.1902A=	ENSP00000507700.1:p.Ile634=
ENST00000684331.1:c.2007A=	ENSP00000507431.1:p.Ile669=
ENST00000684463.1:n.645A=
ENST00000684646.1:c.1794A=	ENSP00000507723.1:p.Ile598=
ENST00000309971.9:c.2007A= MANE Select	ENSP00000308622.5:p.Ile669=
ENST00000309971.8:c.2007A=	ENSP00000308622.4:p.Ile669=
NM_001003722.1:c.2007A= , LRG_484t1:c.2007A=	NP_001003722.1:p.Ile669=
XM_006717059.2:c.2043A=	XP_006717122.1:p.Ile681=
XM_006717060.2:c.2016A=	XP_006717123.1:p.Ile672=
XM_011518549.1:c.2043A=	XP_011516851.1:p.Ile681=
XM_011518550.1:c.2043A=	XP_011516852.1:p.Ile681=
XM_011518551.1:c.2034A=	XP_011516853.1:p.Ile678=
XM_011518552.1:c.1284A=	XP_011516854.1:p.Ile428=
XR_242681.3:n.100+3062T=
XR_428600.2:n.124+653T=
XM_006717059.3:c.2043A=	XP_006717122.1:p.Ile681=
XM_006717060.3:c.2016A=	XP_006717123.1:p.Ile672=
XM_011518551.2:c.2034A=	XP_011516853.1:p.Ile678=
XM_024447519.1:c.2016A=	XP_024303287.1:p.Ile672=
XR_428600.3:n.126+653T=
NM_001003722.2:c.2007A= MANE Select	NP_001003722.1:p.Ile669=