Canonical Allele Identifier: CA1880333338

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541157T= , CM000671.2:g.128541157T=	GRCh38
NC_000009.11:g.131303436T= , CM000671.1:g.131303436T=	GRCh37
NC_000009.10:g.130343257T=	NCBI36
NG_012073.1:g.41466T= , LRG_484:g.41466T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1155T=	ENSP00000507095.1:n.*1155T=
ENST00000683288.1:c.*2083T=	ENSP00000507477.1:n.*2083T=
ENST00000683748.1:c.2111T=	ENSP00000507377.1:p.Phe704=
ENST00000683905.1:c.*760T=	ENSP00000506960.1:n.*760T=
ENST00000684139.1:c.1619T=	ENSP00000507295.1:p.Phe540=
ENST00000684210.1:n.1797T=
ENST00000684314.1:c.1979T=	ENSP00000507700.1:p.Phe660=
ENST00000684331.1:c.*804T=	ENSP00000507431.1:n.*804T=
ENST00000684463.1:n.722T=
ENST00000684646.1:c.1871T=	ENSP00000507723.1:p.Phe624=
ENST00000309971.9:c.2084T= MANE Select	ENSP00000308622.5:p.Phe695=
ENST00000309971.8:c.2084T=	ENSP00000308622.4:p.Phe695=
NM_001003722.1:c.2084T= , LRG_484t1:c.2084T=	NP_001003722.1:p.Phe695=
XM_006717059.2:c.2120T=	XP_006717122.1:p.Phe707=
XM_006717060.2:c.2093T=	XP_006717123.1:p.Phe698=
XM_011518549.1:c.2120T=	XP_011516851.1:p.Phe707=
XM_011518550.1:c.2120T=	XP_011516852.1:p.Phe707=
XM_011518551.1:c.2111T=	XP_011516853.1:p.Phe704=
XM_011518552.1:c.1361T=	XP_011516854.1:p.Phe454=
XR_242681.3:n.100+2222A=
XM_006717059.3:c.2120T=	XP_006717122.1:p.Phe707=
XM_006717060.3:c.2093T=	XP_006717123.1:p.Phe698=
XM_011518551.2:c.2111T=	XP_011516853.1:p.Phe704=
XM_024447519.1:c.2093T=	XP_024303287.1:p.Phe698=
NM_001003722.2:c.2084T= MANE Select	NP_001003722.1:p.Phe695=