Canonical Allele Identifier: CA1880332311

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540318C= , CM000671.2:g.128540318C=	GRCh38
NC_000009.11:g.131302597C= , CM000671.1:g.131302597C=	GRCh37
NC_000009.10:g.130342418C=	NCBI36
NG_012073.1:g.40627C= , LRG_484:g.40627C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1079C=	ENSP00000507095.1:n.*1079C=
ENST00000683288.1:c.*2007C=	ENSP00000507477.1:n.*2007C=
ENST00000683748.1:c.2035C=	ENSP00000507377.1:p.Arg679=
ENST00000683905.1:c.*684C=	ENSP00000506960.1:n.*684C=
ENST00000684139.1:c.1543C=	ENSP00000507295.1:p.Arg515=
ENST00000684210.1:n.1721C=
ENST00000684314.1:c.1903C=	ENSP00000507700.1:p.Arg635=
ENST00000684331.1:c.2008C=	ENSP00000507431.1:p.Arg670=
ENST00000684463.1:n.646C=
ENST00000684646.1:c.1795C=	ENSP00000507723.1:p.Arg599=
ENST00000309971.9:c.2008C= MANE Select	ENSP00000308622.5:p.Arg670=
ENST00000309971.8:c.2008C=	ENSP00000308622.4:p.Arg670=
NM_001003722.1:c.2008C= , LRG_484t1:c.2008C=	NP_001003722.1:p.Arg670=
XM_006717059.2:c.2044C=	XP_006717122.1:p.Arg682=
XM_006717060.2:c.2017C=	XP_006717123.1:p.Arg673=
XM_011518549.1:c.2044C=	XP_011516851.1:p.Arg682=
XM_011518550.1:c.2044C=	XP_011516852.1:p.Arg682=
XM_011518551.1:c.2035C=	XP_011516853.1:p.Arg679=
XM_011518552.1:c.1285C=	XP_011516854.1:p.Arg429=
XR_242681.3:n.100+3061G=
XR_428600.2:n.124+652G=
XM_006717059.3:c.2044C=	XP_006717122.1:p.Arg682=
XM_006717060.3:c.2017C=	XP_006717123.1:p.Arg673=
XM_011518551.2:c.2035C=	XP_011516853.1:p.Arg679=
XM_024447519.1:c.2017C=	XP_024303287.1:p.Arg673=
XR_428600.3:n.126+652G=
NM_001003722.2:c.2008C= MANE Select	NP_001003722.1:p.Arg670=