Canonical Allele Identifier: CA1880333369

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541169G= , CM000671.2:g.128541169G=	GRCh38
NC_000009.11:g.131303448G= , CM000671.1:g.131303448G=	GRCh37
NC_000009.10:g.130343269G=	NCBI36
NG_012073.1:g.41478G= , LRG_484:g.41478G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1167G=	ENSP00000507095.1:n.*1167G=
ENST00000683288.1:c.*2095G=	ENSP00000507477.1:n.*2095G=
ENST00000683748.1:c.2123G=	ENSP00000507377.1:p.Ter708=
ENST00000683905.1:c.*772G=	ENSP00000506960.1:n.*772G=
ENST00000684139.1:c.1631G=	ENSP00000507295.1:p.Ter544=
ENST00000684210.1:n.1809G=
ENST00000684314.1:c.1991G=	ENSP00000507700.1:p.Ter664=
ENST00000684331.1:c.*816G=	ENSP00000507431.1:n.*816G=
ENST00000684463.1:n.734G=
ENST00000684646.1:c.1883G=	ENSP00000507723.1:p.Ter628=
ENST00000309971.9:c.2096G= MANE Select	ENSP00000308622.5:p.Ter699=
ENST00000309971.8:c.2096G=	ENSP00000308622.4:p.Ter699=
NM_001003722.1:c.2096G= , LRG_484t1:c.2096G=	NP_001003722.1:p.Ter699=
XM_006717059.2:c.2132G=	XP_006717122.1:p.Ter711=
XM_006717060.2:c.2105G=	XP_006717123.1:p.Ter702=
XM_011518549.1:c.2132G=	XP_011516851.1:p.Ter711=
XM_011518550.1:c.2132G=	XP_011516852.1:p.Ter711=
XM_011518551.1:c.2123G=	XP_011516853.1:p.Ter708=
XM_011518552.1:c.1373G=	XP_011516854.1:p.Ter458=
XR_242681.3:n.100+2210C=
XM_006717059.3:c.2132G=	XP_006717122.1:p.Ter711=
XM_006717060.3:c.2105G=	XP_006717123.1:p.Ter702=
XM_011518551.2:c.2123G=	XP_011516853.1:p.Ter708=
XM_024447519.1:c.2105G=	XP_024303287.1:p.Ter702=
NM_001003722.2:c.2096G= MANE Select	NP_001003722.1:p.Ter699=