Canonical Allele Identifier: CA467289134

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131303478G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541199G>T , CM000671.2:g.128541199G>T	GRCh38
NC_000009.11:g.131303478G>T , CM000671.1:g.131303478G>T	GRCh37
NC_000009.10:g.130343299G>T	NCBI36
NG_012073.1:g.41508G>T , LRG_484:g.41508G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1197G>T	ENSP00000507095.1:n.*1197G>T
ENST00000683288.1:c.*2125G>T	ENSP00000507477.1:n.*2125G>T
ENST00000683748.1:c.*29G>T	ENSP00000507377.1:n.*29G>T
ENST00000683905.1:c.*802G>T	ENSP00000506960.1:n.*802G>T
ENST00000684139.1:c.*29G>T	ENSP00000507295.1:n.*29G>T
ENST00000684210.1:n.1839G>T
ENST00000684314.1:c.*29G>T	ENSP00000507700.1:n.*29G>T
ENST00000684331.1:c.*846G>T	ENSP00000507431.1:n.*846G>T
ENST00000684463.1:n.764G>T
ENST00000684646.1:c.*29G>T	ENSP00000507723.1:n.*29G>T
ENST00000309971.9:c.*29G>T MANE Select	ENSP00000308622.5:n.*29G>T
ENST00000309971.8:c.*29G>T	ENSP00000308622.4:n.*29G>T
NM_001003722.1:c.*29G>T , LRG_484t1:c.*29G>T	NP_001003722.1:n.*29G>T
XM_006717059.2:c.*29G>T	XP_006717122.1:n.*29G>T
XM_006717060.2:c.*29G>T	XP_006717123.1:n.*29G>T
XM_011518549.1:c.*29G>T	XP_011516851.1:n.*29G>T
XM_011518550.1:c.*29G>T	XP_011516852.1:n.*29G>T
XM_011518551.1:c.*29G>T	XP_011516853.1:n.*29G>T
XM_011518552.1:c.*29G>T	XP_011516854.1:n.*29G>T
XR_242681.3:n.100+2180C>A
XM_006717059.3:c.*29G>T	XP_006717122.1:n.*29G>T
XM_006717060.3:c.*29G>T	XP_006717123.1:n.*29G>T
XM_011518551.2:c.*29G>T	XP_011516853.1:n.*29G>T
XM_024447519.1:c.*29G>T	XP_024303287.1:n.*29G>T
NM_001003722.2:c.*29G>T MANE Select	NP_001003722.1:n.*29G>T