Canonical Allele Identifier: CA1880332296

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540307G= , CM000671.2:g.128540307G=	GRCh38
NC_000009.11:g.131302586G= , CM000671.1:g.131302586G=	GRCh37
NC_000009.10:g.130342407G=	NCBI36
NG_012073.1:g.40616G= , LRG_484:g.40616G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1068G=	ENSP00000507095.1:n.*1068G=
ENST00000683288.1:c.*1996G=	ENSP00000507477.1:n.*1996G=
ENST00000683748.1:c.2024G=	ENSP00000507377.1:p.Gly675=
ENST00000683905.1:c.*673G=	ENSP00000506960.1:n.*673G=
ENST00000684139.1:c.1532G=	ENSP00000507295.1:p.Gly511=
ENST00000684210.1:n.1710G=
ENST00000684314.1:c.1892G=	ENSP00000507700.1:p.Gly631=
ENST00000684331.1:c.1997G=	ENSP00000507431.1:p.Gly666=
ENST00000684463.1:n.635G=
ENST00000684646.1:c.1784G=	ENSP00000507723.1:p.Gly595=
ENST00000309971.9:c.1997G= MANE Select	ENSP00000308622.5:p.Gly666=
ENST00000309971.8:c.1997G=	ENSP00000308622.4:p.Gly666=
NM_001003722.1:c.1997G= , LRG_484t1:c.1997G=	NP_001003722.1:p.Gly666=
XM_006717059.2:c.2033G=	XP_006717122.1:p.Gly678=
XM_006717060.2:c.2006G=	XP_006717123.1:p.Gly669=
XM_011518549.1:c.2033G=	XP_011516851.1:p.Gly678=
XM_011518550.1:c.2033G=	XP_011516852.1:p.Gly678=
XM_011518551.1:c.2024G=	XP_011516853.1:p.Gly675=
XM_011518552.1:c.1274G=	XP_011516854.1:p.Gly425=
XR_242681.3:n.100+3072C=
XR_428600.2:n.124+663C=
XM_006717059.3:c.2033G=	XP_006717122.1:p.Gly678=
XM_006717060.3:c.2006G=	XP_006717123.1:p.Gly669=
XM_011518551.2:c.2024G=	XP_011516853.1:p.Gly675=
XM_024447519.1:c.2006G=	XP_024303287.1:p.Gly669=
XR_428600.3:n.126+663C=
NM_001003722.2:c.1997G= MANE Select	NP_001003722.1:p.Gly666=