Canonical Allele Identifier: CA1880333313

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541142T= , CM000671.2:g.128541142T=	GRCh38
NC_000009.11:g.131303421T= , CM000671.1:g.131303421T=	GRCh37
NC_000009.10:g.130343242T=	NCBI36
NG_012073.1:g.41451T= , LRG_484:g.41451T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1140T=	ENSP00000507095.1:n.*1140T=
ENST00000683288.1:c.*2068T=	ENSP00000507477.1:n.*2068T=
ENST00000683748.1:c.2096T=	ENSP00000507377.1:p.Phe699=
ENST00000683905.1:c.*745T=	ENSP00000506960.1:n.*745T=
ENST00000684139.1:c.1604T=	ENSP00000507295.1:p.Phe535=
ENST00000684210.1:n.1782T=
ENST00000684314.1:c.1964T=	ENSP00000507700.1:p.Phe655=
ENST00000684331.1:c.*789T=	ENSP00000507431.1:n.*789T=
ENST00000684463.1:n.707T=
ENST00000684646.1:c.1856T=	ENSP00000507723.1:p.Phe619=
ENST00000309971.9:c.2069T= MANE Select	ENSP00000308622.5:p.Phe690=
ENST00000309971.8:c.2069T=	ENSP00000308622.4:p.Phe690=
NM_001003722.1:c.2069T= , LRG_484t1:c.2069T=	NP_001003722.1:p.Phe690=
XM_006717059.2:c.2105T=	XP_006717122.1:p.Phe702=
XM_006717060.2:c.2078T=	XP_006717123.1:p.Phe693=
XM_011518549.1:c.2105T=	XP_011516851.1:p.Phe702=
XM_011518550.1:c.2105T=	XP_011516852.1:p.Phe702=
XM_011518551.1:c.2096T=	XP_011516853.1:p.Phe699=
XM_011518552.1:c.1346T=	XP_011516854.1:p.Phe449=
XR_242681.3:n.100+2237A=
XM_006717059.3:c.2105T=	XP_006717122.1:p.Phe702=
XM_006717060.3:c.2078T=	XP_006717123.1:p.Phe693=
XM_011518551.2:c.2096T=	XP_011516853.1:p.Phe699=
XM_024447519.1:c.2078T=	XP_024303287.1:p.Phe693=
NM_001003722.2:c.2069T= MANE Select	NP_001003722.1:p.Phe690=