Canonical Allele Identifier: CA1880333020

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540816C= , CM000671.2:g.128540816C=	GRCh38
NC_000009.11:g.131303095C= , CM000671.1:g.131303095C=	GRCh37
NC_000009.10:g.130342916C=	NCBI36
NG_012073.1:g.41125C= , LRG_484:g.41125C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1100-286C=	ENSP00000507095.1:n.*1100-286C=
ENST00000683288.1:c.*2028-286C=	ENSP00000507477.1:n.*2028-286C=
ENST00000683748.1:c.2056-286C=	ENSP00000507377.1:n.2056-286C=
ENST00000683905.1:c.*705-286C=	ENSP00000506960.1:n.*705-286C=
ENST00000684139.1:c.1564-286C=	ENSP00000507295.1:n.1564-286C=
ENST00000684210.1:n.1742-286C=
ENST00000684314.1:c.1924-286C=	ENSP00000507700.1:n.1924-286C=
ENST00000684331.1:c.*463C=	ENSP00000507431.1:n.*463C=
ENST00000684463.1:n.667-286C=
ENST00000684646.1:c.1816-286C=	ENSP00000507723.1:n.1816-286C=
ENST00000309971.9:c.2029-286C= MANE Select	ENSP00000308622.5:n.2029-286C=
ENST00000309971.8:c.2029-286C=	ENSP00000308622.4:n.2029-286C=
NM_001003722.1:c.2029-286C= , LRG_484t1:c.2029-286C=	NP_001003722.1:n.2029-286C=
XM_006717059.2:c.2065-286C=	XP_006717122.1:n.2065-286C=
XM_006717060.2:c.2038-286C=	XP_006717123.1:n.2038-286C=
XM_011518549.1:c.2065-286C=	XP_011516851.1:n.2065-286C=
XM_011518550.1:c.2065-286C=	XP_011516852.1:n.2065-286C=
XM_011518551.1:c.2056-286C=	XP_011516853.1:n.2056-286C=
XM_011518552.1:c.1306-286C=	XP_011516854.1:n.1306-286C=
XR_242681.3:n.100+2563G=
XR_428600.2:n.124+154G=
XM_006717059.3:c.2065-286C=	XP_006717122.1:n.2065-286C=
XM_006717060.3:c.2038-286C=	XP_006717123.1:n.2038-286C=
XM_011518551.2:c.2056-286C=	XP_011516853.1:n.2056-286C=
XM_024447519.1:c.2038-286C=	XP_024303287.1:n.2038-286C=
XR_428600.3:n.126+154G=
NM_001003722.2:c.2029-286C= MANE Select	NP_001003722.1:n.2029-286C=