Canonical Allele Identifier: CA1880333408

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541195C= , CM000671.2:g.128541195C=	GRCh38
NC_000009.11:g.131303474C= , CM000671.1:g.131303474C=	GRCh37
NC_000009.10:g.130343295C=	NCBI36
NG_012073.1:g.41504C= , LRG_484:g.41504C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1193C=	ENSP00000507095.1:n.*1193C=
ENST00000683288.1:c.*2121C=	ENSP00000507477.1:n.*2121C=
ENST00000683748.1:c.*25C=	ENSP00000507377.1:n.*25C=
ENST00000683905.1:c.*798C=	ENSP00000506960.1:n.*798C=
ENST00000684139.1:c.*25C=	ENSP00000507295.1:n.*25C=
ENST00000684210.1:n.1835C=
ENST00000684314.1:c.*25C=	ENSP00000507700.1:n.*25C=
ENST00000684331.1:c.*842C=	ENSP00000507431.1:n.*842C=
ENST00000684463.1:n.760C=
ENST00000684646.1:c.*25C=	ENSP00000507723.1:n.*25C=
ENST00000309971.9:c.*25C= MANE Select	ENSP00000308622.5:n.*25C=
ENST00000309971.8:c.*25C=	ENSP00000308622.4:n.*25C=
NM_001003722.1:c.*25C= , LRG_484t1:c.*25C=	NP_001003722.1:n.*25C=
XM_006717059.2:c.*25C=	XP_006717122.1:n.*25C=
XM_006717060.2:c.*25C=	XP_006717123.1:n.*25C=
XM_011518549.1:c.*25C=	XP_011516851.1:n.*25C=
XM_011518550.1:c.*25C=	XP_011516852.1:n.*25C=
XM_011518551.1:c.*25C=	XP_011516853.1:n.*25C=
XM_011518552.1:c.*25C=	XP_011516854.1:n.*25C=
XR_242681.3:n.100+2184G=
XM_006717059.3:c.*25C=	XP_006717122.1:n.*25C=
XM_006717060.3:c.*25C=	XP_006717123.1:n.*25C=
XM_011518551.2:c.*25C=	XP_011516853.1:n.*25C=
XM_024447519.1:c.*25C=	XP_024303287.1:n.*25C=
NM_001003722.2:c.*25C= MANE Select	NP_001003722.1:n.*25C=