Canonical Allele Identifier: CA1880333285

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541121A= , CM000671.2:g.128541121A=	GRCh38
NC_000009.11:g.131303400A= , CM000671.1:g.131303400A=	GRCh37
NC_000009.10:g.130343221A=	NCBI36
NG_012073.1:g.41430A= , LRG_484:g.41430A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1119A=	ENSP00000507095.1:n.*1119A=
ENST00000683288.1:c.*2047A=	ENSP00000507477.1:n.*2047A=
ENST00000683748.1:c.2075A=	ENSP00000507377.1:p.Asp692=
ENST00000683905.1:c.*724A=	ENSP00000506960.1:n.*724A=
ENST00000684139.1:c.1583A=	ENSP00000507295.1:p.Asp528=
ENST00000684210.1:n.1761A=
ENST00000684314.1:c.1943A=	ENSP00000507700.1:p.Asp648=
ENST00000684331.1:c.*768A=	ENSP00000507431.1:n.*768A=
ENST00000684463.1:n.686A=
ENST00000684646.1:c.1835A=	ENSP00000507723.1:p.Asp612=
ENST00000309971.9:c.2048A= MANE Select	ENSP00000308622.5:p.Asp683=
ENST00000309971.8:c.2048A=	ENSP00000308622.4:p.Asp683=
NM_001003722.1:c.2048A= , LRG_484t1:c.2048A=	NP_001003722.1:p.Asp683=
XM_006717059.2:c.2084A=	XP_006717122.1:p.Asp695=
XM_006717060.2:c.2057A=	XP_006717123.1:p.Asp686=
XM_011518549.1:c.2084A=	XP_011516851.1:p.Asp695=
XM_011518550.1:c.2084A=	XP_011516852.1:p.Asp695=
XM_011518551.1:c.2075A=	XP_011516853.1:p.Asp692=
XM_011518552.1:c.1325A=	XP_011516854.1:p.Asp442=
XR_242681.3:n.100+2258T=
XM_006717059.3:c.2084A=	XP_006717122.1:p.Asp695=
XM_006717060.3:c.2057A=	XP_006717123.1:p.Asp686=
XM_011518551.2:c.2075A=	XP_011516853.1:p.Asp692=
XM_024447519.1:c.2057A=	XP_024303287.1:p.Asp686=
NM_001003722.2:c.2048A= MANE Select	NP_001003722.1:p.Asp683=