Canonical Allele Identifier: CA1880333283

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541117A= , CM000671.2:g.128541117A=	GRCh38
NC_000009.11:g.131303396A= , CM000671.1:g.131303396A=	GRCh37
NC_000009.10:g.130343217A=	NCBI36
NG_012073.1:g.41426A= , LRG_484:g.41426A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1115A=	ENSP00000507095.1:n.*1115A=
ENST00000683288.1:c.*2043A=	ENSP00000507477.1:n.*2043A=
ENST00000683748.1:c.2071A=	ENSP00000507377.1:p.Lys691=
ENST00000683905.1:c.*720A=	ENSP00000506960.1:n.*720A=
ENST00000684139.1:c.1579A=	ENSP00000507295.1:p.Lys527=
ENST00000684210.1:n.1757A=
ENST00000684314.1:c.1939A=	ENSP00000507700.1:p.Lys647=
ENST00000684331.1:c.*764A=	ENSP00000507431.1:n.*764A=
ENST00000684463.1:n.682A=
ENST00000684646.1:c.1831A=	ENSP00000507723.1:p.Lys611=
ENST00000309971.9:c.2044A= MANE Select	ENSP00000308622.5:p.Lys682=
ENST00000309971.8:c.2044A=	ENSP00000308622.4:p.Lys682=
NM_001003722.1:c.2044A= , LRG_484t1:c.2044A=	NP_001003722.1:p.Lys682=
XM_006717059.2:c.2080A=	XP_006717122.1:p.Lys694=
XM_006717060.2:c.2053A=	XP_006717123.1:p.Lys685=
XM_011518549.1:c.2080A=	XP_011516851.1:p.Lys694=
XM_011518550.1:c.2080A=	XP_011516852.1:p.Lys694=
XM_011518551.1:c.2071A=	XP_011516853.1:p.Lys691=
XM_011518552.1:c.1321A=	XP_011516854.1:p.Lys441=
XR_242681.3:n.100+2262T=
XM_006717059.3:c.2080A=	XP_006717122.1:p.Lys694=
XM_006717060.3:c.2053A=	XP_006717123.1:p.Lys685=
XM_011518551.2:c.2071A=	XP_011516853.1:p.Lys691=
XM_024447519.1:c.2053A=	XP_024303287.1:p.Lys685=
NM_001003722.2:c.2044A= MANE Select	NP_001003722.1:p.Lys682=