Canonical Allele Identifier: CA467289129

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131303476C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541197C>G , CM000671.2:g.128541197C>G	GRCh38
NC_000009.11:g.131303476C>G , CM000671.1:g.131303476C>G	GRCh37
NC_000009.10:g.130343297C>G	NCBI36
NG_012073.1:g.41506C>G , LRG_484:g.41506C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1195C>G	ENSP00000507095.1:n.*1195C>G
ENST00000683288.1:c.*2123C>G	ENSP00000507477.1:n.*2123C>G
ENST00000683748.1:c.*27C>G	ENSP00000507377.1:n.*27C>G
ENST00000683905.1:c.*800C>G	ENSP00000506960.1:n.*800C>G
ENST00000684139.1:c.*27C>G	ENSP00000507295.1:n.*27C>G
ENST00000684210.1:n.1837C>G
ENST00000684314.1:c.*27C>G	ENSP00000507700.1:n.*27C>G
ENST00000684331.1:c.*844C>G	ENSP00000507431.1:n.*844C>G
ENST00000684463.1:n.762C>G
ENST00000684646.1:c.*27C>G	ENSP00000507723.1:n.*27C>G
ENST00000309971.9:c.*27C>G MANE Select	ENSP00000308622.5:n.*27C>G
ENST00000309971.8:c.*27C>G	ENSP00000308622.4:n.*27C>G
NM_001003722.1:c.*27C>G , LRG_484t1:c.*27C>G	NP_001003722.1:n.*27C>G
XM_006717059.2:c.*27C>G	XP_006717122.1:n.*27C>G
XM_006717060.2:c.*27C>G	XP_006717123.1:n.*27C>G
XM_011518549.1:c.*27C>G	XP_011516851.1:n.*27C>G
XM_011518550.1:c.*27C>G	XP_011516852.1:n.*27C>G
XM_011518551.1:c.*27C>G	XP_011516853.1:n.*27C>G
XM_011518552.1:c.*27C>G	XP_011516854.1:n.*27C>G
XR_242681.3:n.100+2182G>C
XM_006717059.3:c.*27C>G	XP_006717122.1:n.*27C>G
XM_006717060.3:c.*27C>G	XP_006717123.1:n.*27C>G
XM_011518551.2:c.*27C>G	XP_011516853.1:n.*27C>G
XM_024447519.1:c.*27C>G	XP_024303287.1:n.*27C>G
NM_001003722.2:c.*27C>G MANE Select	NP_001003722.1:n.*27C>G