Canonical Allele Identifier: CA1880333270

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541104A= , CM000671.2:g.128541104A=	GRCh38
NC_000009.11:g.131303383A= , CM000671.1:g.131303383A=	GRCh37
NC_000009.10:g.130343204A=	NCBI36
NG_012073.1:g.41413A= , LRG_484:g.41413A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1102A=	ENSP00000507095.1:n.*1102A=
ENST00000683288.1:c.*2030A=	ENSP00000507477.1:n.*2030A=
ENST00000683748.1:c.2058A=	ENSP00000507377.1:p.Lys686=
ENST00000683905.1:c.*707A=	ENSP00000506960.1:n.*707A=
ENST00000684139.1:c.1566A=	ENSP00000507295.1:p.Lys522=
ENST00000684210.1:n.1744A=
ENST00000684314.1:c.1926A=	ENSP00000507700.1:p.Lys642=
ENST00000684331.1:c.*751A=	ENSP00000507431.1:n.*751A=
ENST00000684463.1:n.669A=
ENST00000684646.1:c.1818A=	ENSP00000507723.1:p.Lys606=
ENST00000309971.9:c.2031A= MANE Select	ENSP00000308622.5:p.Lys677=
ENST00000309971.8:c.2031A=	ENSP00000308622.4:p.Lys677=
NM_001003722.1:c.2031A= , LRG_484t1:c.2031A=	NP_001003722.1:p.Lys677=
XM_006717059.2:c.2067A=	XP_006717122.1:p.Lys689=
XM_006717060.2:c.2040A=	XP_006717123.1:p.Lys680=
XM_011518549.1:c.2067A=	XP_011516851.1:p.Lys689=
XM_011518550.1:c.2067A=	XP_011516852.1:p.Lys689=
XM_011518551.1:c.2058A=	XP_011516853.1:p.Lys686=
XM_011518552.1:c.1308A=	XP_011516854.1:p.Lys436=
XR_242681.3:n.100+2275T=
XM_006717059.3:c.2067A=	XP_006717122.1:p.Lys689=
XM_006717060.3:c.2040A=	XP_006717123.1:p.Lys680=
XM_011518551.2:c.2058A=	XP_011516853.1:p.Lys686=
XM_024447519.1:c.2040A=	XP_024303287.1:p.Lys680=
NM_001003722.2:c.2031A= MANE Select	NP_001003722.1:p.Lys677=