Canonical Allele Identifier: CA1880332288

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540277T= , CM000671.2:g.128540277T=	GRCh38
NC_000009.11:g.131302556T= , CM000671.1:g.131302556T=	GRCh37
NC_000009.10:g.130342377T=	NCBI36
NG_012073.1:g.40586T= , LRG_484:g.40586T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1038T=	ENSP00000507095.1:n.*1038T=
ENST00000683288.1:c.*1966T=	ENSP00000507477.1:n.*1966T=
ENST00000683748.1:c.1994T=	ENSP00000507377.1:p.Ile665=
ENST00000683905.1:c.*643T=	ENSP00000506960.1:n.*643T=
ENST00000684139.1:c.1502T=	ENSP00000507295.1:p.Ile501=
ENST00000684210.1:n.1680T=
ENST00000684314.1:c.1862T=	ENSP00000507700.1:p.Ile621=
ENST00000684331.1:c.1967T=	ENSP00000507431.1:p.Ile656=
ENST00000684463.1:n.605T=
ENST00000684646.1:c.1754T=	ENSP00000507723.1:p.Ile585=
ENST00000309971.9:c.1967T= MANE Select	ENSP00000308622.5:p.Ile656=
ENST00000309971.8:c.1967T=	ENSP00000308622.4:p.Ile656=
NM_001003722.1:c.1967T= , LRG_484t1:c.1967T=	NP_001003722.1:p.Ile656=
XM_006717059.2:c.2003T=	XP_006717122.1:p.Ile668=
XM_006717060.2:c.1976T=	XP_006717123.1:p.Ile659=
XM_011518549.1:c.2003T=	XP_011516851.1:p.Ile668=
XM_011518550.1:c.2003T=	XP_011516852.1:p.Ile668=
XM_011518551.1:c.1994T=	XP_011516853.1:p.Ile665=
XM_011518552.1:c.1244T=	XP_011516854.1:p.Ile415=
XR_242681.3:n.100+3102A=
XR_428600.2:n.124+693A=
XM_006717059.3:c.2003T=	XP_006717122.1:p.Ile668=
XM_006717060.3:c.1976T=	XP_006717123.1:p.Ile659=
XM_011518551.2:c.1994T=	XP_011516853.1:p.Ile665=
XM_024447519.1:c.1976T=	XP_024303287.1:p.Ile659=
XR_428600.3:n.126+693A=
NM_001003722.2:c.1967T= MANE Select	NP_001003722.1:p.Ile656=