Canonical Allele Identifier: CA467289089

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131303462A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541183A>T , CM000671.2:g.128541183A>T	GRCh38
NC_000009.11:g.131303462A>T , CM000671.1:g.131303462A>T	GRCh37
NC_000009.10:g.130343283A>T	NCBI36
NG_012073.1:g.41492A>T , LRG_484:g.41492A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1181A>T	ENSP00000507095.1:n.*1181A>T
ENST00000683288.1:c.*2109A>T	ENSP00000507477.1:n.*2109A>T
ENST00000683748.1:c.*13A>T	ENSP00000507377.1:n.*13A>T
ENST00000683905.1:c.*786A>T	ENSP00000506960.1:n.*786A>T
ENST00000684139.1:c.*13A>T	ENSP00000507295.1:n.*13A>T
ENST00000684210.1:n.1823A>T
ENST00000684314.1:c.*13A>T	ENSP00000507700.1:n.*13A>T
ENST00000684331.1:c.*830A>T	ENSP00000507431.1:n.*830A>T
ENST00000684463.1:n.748A>T
ENST00000684646.1:c.*13A>T	ENSP00000507723.1:n.*13A>T
ENST00000309971.9:c.*13A>T MANE Select	ENSP00000308622.5:n.*13A>T
ENST00000309971.8:c.*13A>T	ENSP00000308622.4:n.*13A>T
NM_001003722.1:c.*13A>T , LRG_484t1:c.*13A>T	NP_001003722.1:n.*13A>T
XM_006717059.2:c.*13A>T	XP_006717122.1:n.*13A>T
XM_006717060.2:c.*13A>T	XP_006717123.1:n.*13A>T
XM_011518549.1:c.*13A>T	XP_011516851.1:n.*13A>T
XM_011518550.1:c.*13A>T	XP_011516852.1:n.*13A>T
XM_011518551.1:c.*13A>T	XP_011516853.1:n.*13A>T
XM_011518552.1:c.*13A>T	XP_011516854.1:n.*13A>T
XR_242681.3:n.100+2196T>A
XM_006717059.3:c.*13A>T	XP_006717122.1:n.*13A>T
XM_006717060.3:c.*13A>T	XP_006717123.1:n.*13A>T
XM_011518551.2:c.*13A>T	XP_011516853.1:n.*13A>T
XM_024447519.1:c.*13A>T	XP_024303287.1:n.*13A>T
NM_001003722.2:c.*13A>T MANE Select	NP_001003722.1:n.*13A>T