Canonical Allele Identifier: CA1880333399

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541182C= , CM000671.2:g.128541182C=	GRCh38
NC_000009.11:g.131303461C= , CM000671.1:g.131303461C=	GRCh37
NC_000009.10:g.130343282C=	NCBI36
NG_012073.1:g.41491C= , LRG_484:g.41491C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1180C=	ENSP00000507095.1:n.*1180C=
ENST00000683288.1:c.*2108C=	ENSP00000507477.1:n.*2108C=
ENST00000683748.1:c.*12C=	ENSP00000507377.1:n.*12C=
ENST00000683905.1:c.*785C=	ENSP00000506960.1:n.*785C=
ENST00000684139.1:c.*12C=	ENSP00000507295.1:n.*12C=
ENST00000684210.1:n.1822C=
ENST00000684314.1:c.*12C=	ENSP00000507700.1:n.*12C=
ENST00000684331.1:c.*829C=	ENSP00000507431.1:n.*829C=
ENST00000684463.1:n.747C=
ENST00000684646.1:c.*12C=	ENSP00000507723.1:n.*12C=
ENST00000309971.9:c.*12C= MANE Select	ENSP00000308622.5:n.*12C=
ENST00000309971.8:c.*12C=	ENSP00000308622.4:n.*12C=
NM_001003722.1:c.*12C= , LRG_484t1:c.*12C=	NP_001003722.1:n.*12C=
XM_006717059.2:c.*12C=	XP_006717122.1:n.*12C=
XM_006717060.2:c.*12C=	XP_006717123.1:n.*12C=
XM_011518549.1:c.*12C=	XP_011516851.1:n.*12C=
XM_011518550.1:c.*12C=	XP_011516852.1:n.*12C=
XM_011518551.1:c.*12C=	XP_011516853.1:n.*12C=
XM_011518552.1:c.*12C=	XP_011516854.1:n.*12C=
XR_242681.3:n.100+2197G=
XM_006717059.3:c.*12C=	XP_006717122.1:n.*12C=
XM_006717060.3:c.*12C=	XP_006717123.1:n.*12C=
XM_011518551.2:c.*12C=	XP_011516853.1:n.*12C=
XM_024447519.1:c.*12C=	XP_024303287.1:n.*12C=
NM_001003722.2:c.*12C= MANE Select	NP_001003722.1:n.*12C=