Canonical Allele Identifier: CA1880333327

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541154C= , CM000671.2:g.128541154C=	GRCh38
NC_000009.11:g.131303433C= , CM000671.1:g.131303433C=	GRCh37
NC_000009.10:g.130343254C=	NCBI36
NG_012073.1:g.41463C= , LRG_484:g.41463C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1152C=	ENSP00000507095.1:n.*1152C=
ENST00000683288.1:c.*2080C=	ENSP00000507477.1:n.*2080C=
ENST00000683748.1:c.2108C=	ENSP00000507377.1:p.Ser703=
ENST00000683905.1:c.*757C=	ENSP00000506960.1:n.*757C=
ENST00000684139.1:c.1616C=	ENSP00000507295.1:p.Ser539=
ENST00000684210.1:n.1794C=
ENST00000684314.1:c.1976C=	ENSP00000507700.1:p.Ser659=
ENST00000684331.1:c.*801C=	ENSP00000507431.1:n.*801C=
ENST00000684463.1:n.719C=
ENST00000684646.1:c.1868C=	ENSP00000507723.1:p.Ser623=
ENST00000309971.9:c.2081C= MANE Select	ENSP00000308622.5:p.Ser694=
ENST00000309971.8:c.2081C=	ENSP00000308622.4:p.Ser694=
NM_001003722.1:c.2081C= , LRG_484t1:c.2081C=	NP_001003722.1:p.Ser694=
XM_006717059.2:c.2117C=	XP_006717122.1:p.Ser706=
XM_006717060.2:c.2090C=	XP_006717123.1:p.Ser697=
XM_011518549.1:c.2117C=	XP_011516851.1:p.Ser706=
XM_011518550.1:c.2117C=	XP_011516852.1:p.Ser706=
XM_011518551.1:c.2108C=	XP_011516853.1:p.Ser703=
XM_011518552.1:c.1358C=	XP_011516854.1:p.Ser453=
XR_242681.3:n.100+2225G=
XM_006717059.3:c.2117C=	XP_006717122.1:p.Ser706=
XM_006717060.3:c.2090C=	XP_006717123.1:p.Ser697=
XM_011518551.2:c.2108C=	XP_011516853.1:p.Ser703=
XM_024447519.1:c.2090C=	XP_024303287.1:p.Ser697=
NM_001003722.2:c.2081C= MANE Select	NP_001003722.1:p.Ser694=