Canonical Allele Identifier: CA467289133

Gene: GLE1

Linked Data

• gnomAD v4: 9-128541198-T-G
• MyVariant Identifiers: chr9:g.131303477T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541198T>G , CM000671.2:g.128541198T>G	GRCh38
NC_000009.11:g.131303477T>G , CM000671.1:g.131303477T>G	GRCh37
NC_000009.10:g.130343298T>G	NCBI36
NG_012073.1:g.41507T>G , LRG_484:g.41507T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1196T>G	ENSP00000507095.1:n.*1196T>G
ENST00000683288.1:c.*2124T>G	ENSP00000507477.1:n.*2124T>G
ENST00000683748.1:c.*28T>G	ENSP00000507377.1:n.*28T>G
ENST00000683905.1:c.*801T>G	ENSP00000506960.1:n.*801T>G
ENST00000684139.1:c.*28T>G	ENSP00000507295.1:n.*28T>G
ENST00000684210.1:n.1838T>G
ENST00000684314.1:c.*28T>G	ENSP00000507700.1:n.*28T>G
ENST00000684331.1:c.*845T>G	ENSP00000507431.1:n.*845T>G
ENST00000684463.1:n.763T>G
ENST00000684646.1:c.*28T>G	ENSP00000507723.1:n.*28T>G
ENST00000309971.9:c.*28T>G MANE Select	ENSP00000308622.5:n.*28T>G
ENST00000309971.8:c.*28T>G	ENSP00000308622.4:n.*28T>G
NM_001003722.1:c.*28T>G , LRG_484t1:c.*28T>G	NP_001003722.1:n.*28T>G
XM_006717059.2:c.*28T>G	XP_006717122.1:n.*28T>G
XM_006717060.2:c.*28T>G	XP_006717123.1:n.*28T>G
XM_011518549.1:c.*28T>G	XP_011516851.1:n.*28T>G
XM_011518550.1:c.*28T>G	XP_011516852.1:n.*28T>G
XM_011518551.1:c.*28T>G	XP_011516853.1:n.*28T>G
XM_011518552.1:c.*28T>G	XP_011516854.1:n.*28T>G
XR_242681.3:n.100+2181A>C
XM_006717059.3:c.*28T>G	XP_006717122.1:n.*28T>G
XM_006717060.3:c.*28T>G	XP_006717123.1:n.*28T>G
XM_011518551.2:c.*28T>G	XP_011516853.1:n.*28T>G
XM_024447519.1:c.*28T>G	XP_024303287.1:n.*28T>G
NM_001003722.2:c.*28T>G MANE Select	NP_001003722.1:n.*28T>G