Canonical Allele Identifier: CA1880333278

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541116C= , CM000671.2:g.128541116C=	GRCh38
NC_000009.11:g.131303395C= , CM000671.1:g.131303395C=	GRCh37
NC_000009.10:g.130343216C=	NCBI36
NG_012073.1:g.41425C= , LRG_484:g.41425C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1114C=	ENSP00000507095.1:n.*1114C=
ENST00000683288.1:c.*2042C=	ENSP00000507477.1:n.*2042C=
ENST00000683748.1:c.2070C=	ENSP00000507377.1:p.His690=
ENST00000683905.1:c.*719C=	ENSP00000506960.1:n.*719C=
ENST00000684139.1:c.1578C=	ENSP00000507295.1:p.His526=
ENST00000684210.1:n.1756C=
ENST00000684314.1:c.1938C=	ENSP00000507700.1:p.His646=
ENST00000684331.1:c.*763C=	ENSP00000507431.1:n.*763C=
ENST00000684463.1:n.681C=
ENST00000684646.1:c.1830C=	ENSP00000507723.1:p.His610=
ENST00000309971.9:c.2043C= MANE Select	ENSP00000308622.5:p.His681=
ENST00000309971.8:c.2043C=	ENSP00000308622.4:p.His681=
NM_001003722.1:c.2043C= , LRG_484t1:c.2043C=	NP_001003722.1:p.His681=
XM_006717059.2:c.2079C=	XP_006717122.1:p.His693=
XM_006717060.2:c.2052C=	XP_006717123.1:p.His684=
XM_011518549.1:c.2079C=	XP_011516851.1:p.His693=
XM_011518550.1:c.2079C=	XP_011516852.1:p.His693=
XM_011518551.1:c.2070C=	XP_011516853.1:p.His690=
XM_011518552.1:c.1320C=	XP_011516854.1:p.His440=
XR_242681.3:n.100+2263G=
XM_006717059.3:c.2079C=	XP_006717122.1:p.His693=
XM_006717060.3:c.2052C=	XP_006717123.1:p.His684=
XM_011518551.2:c.2070C=	XP_011516853.1:p.His690=
XM_024447519.1:c.2052C=	XP_024303287.1:p.His684=
NM_001003722.2:c.2043C= MANE Select	NP_001003722.1:p.His681=