Canonical Allele Identifier: CA1880317139

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128515918A= , CM000671.2:g.128515918A=	GRCh38
NC_000009.11:g.131278197A= , CM000671.1:g.131278197A=	GRCh37
NC_000009.10:g.130318018A=	NCBI36
NG_012073.1:g.16227A= , LRG_484:g.16227A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001003722.2:c.432+279A= MANE Select	NP_001003722.1:n.432+279A=
ENST00000309971.9:c.432+279A= MANE Select	ENSP00000308622.5:n.432+279A=
NM_001003722.1:c.432+279A= , LRG_484t1:c.432+279A=	NP_001003722.1:n.432+279A=
NM_001499.2:c.432+279A= , LRG_484t2:c.432+279A=	NP_001490.1:n.432+279A=
ENST00000309971.8:c.432+279A=	ENSP00000308622.4:n.432+279A=
ENST00000372770.4:c.432+279A=	ENSP00000361856.4:n.432+279A=
ENST00000494417.2:n.536+279A=
ENST00000682831.1:c.*228A=	ENSP00000508410.1:n.*228A=
ENST00000683044.1:c.432+279A=	ENSP00000507095.1:n.432+279A=
ENST00000683288.1:c.*431+279A=	ENSP00000507477.1:n.*431+279A=
ENST00000683748.1:c.432+279A=	ENSP00000507377.1:n.432+279A=
ENST00000683905.1:c.432+279A=	ENSP00000506960.1:n.432+279A=
ENST00000684139.1:c.432+279A=	ENSP00000507295.1:n.432+279A=
ENST00000684314.1:c.432+279A=	ENSP00000507700.1:n.432+279A=
ENST00000684331.1:c.432+279A=	ENSP00000507431.1:n.432+279A=
ENST00000684646.1:c.432+279A=	ENSP00000507723.1:n.432+279A=
XM_006717059.2:c.441+279A=	XP_006717122.1:n.441+279A=
XM_006717059.3:c.441+279A=	XP_006717122.1:n.441+279A=
XM_006717060.2:c.441+279A=	XP_006717123.1:n.441+279A=
XM_006717060.3:c.441+279A=	XP_006717123.1:n.441+279A=
XM_011518549.1:c.441+279A=	XP_011516851.1:n.441+279A=
XM_011518550.1:c.441+279A=	XP_011516852.1:n.441+279A=
XM_011518551.1:c.432+279A=	XP_011516853.1:n.432+279A=
XM_011518551.2:c.432+279A=	XP_011516853.1:n.432+279A=
XM_011518552.1:c.-314+279A=	XP_011516854.1:n.-314+279A=
XM_024447519.1:c.441+279A=	XP_024303287.1:n.441+279A=