Canonical Allele Identifier: CA1880332294

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540304T= , CM000671.2:g.128540304T=	GRCh38
NC_000009.11:g.131302583T= , CM000671.1:g.131302583T=	GRCh37
NC_000009.10:g.130342404T=	NCBI36
NG_012073.1:g.40613T= , LRG_484:g.40613T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1065T=	ENSP00000507095.1:n.*1065T=
ENST00000683288.1:c.*1993T=	ENSP00000507477.1:n.*1993T=
ENST00000683748.1:c.2021T=	ENSP00000507377.1:p.Met674=
ENST00000683905.1:c.*670T=	ENSP00000506960.1:n.*670T=
ENST00000684139.1:c.1529T=	ENSP00000507295.1:p.Met510=
ENST00000684210.1:n.1707T=
ENST00000684314.1:c.1889T=	ENSP00000507700.1:p.Met630=
ENST00000684331.1:c.1994T=	ENSP00000507431.1:p.Met665=
ENST00000684463.1:n.632T=
ENST00000684646.1:c.1781T=	ENSP00000507723.1:p.Met594=
ENST00000309971.9:c.1994T= MANE Select	ENSP00000308622.5:p.Met665=
ENST00000309971.8:c.1994T=	ENSP00000308622.4:p.Met665=
NM_001003722.1:c.1994T= , LRG_484t1:c.1994T=	NP_001003722.1:p.Met665=
XM_006717059.2:c.2030T=	XP_006717122.1:p.Met677=
XM_006717060.2:c.2003T=	XP_006717123.1:p.Met668=
XM_011518549.1:c.2030T=	XP_011516851.1:p.Met677=
XM_011518550.1:c.2030T=	XP_011516852.1:p.Met677=
XM_011518551.1:c.2021T=	XP_011516853.1:p.Met674=
XM_011518552.1:c.1271T=	XP_011516854.1:p.Met424=
XR_242681.3:n.100+3075A=
XR_428600.2:n.124+666A=
XM_006717059.3:c.2030T=	XP_006717122.1:p.Met677=
XM_006717060.3:c.2003T=	XP_006717123.1:p.Met668=
XM_011518551.2:c.2021T=	XP_011516853.1:p.Met674=
XM_024447519.1:c.2003T=	XP_024303287.1:p.Met668=
XR_428600.3:n.126+666A=
NM_001003722.2:c.1994T= MANE Select	NP_001003722.1:p.Met665=