Canonical Allele Identifier: CA375046339

Gene: GLE1

Linked Data

• gnomAD v4: 9-128541114-C-A
• MyVariant Identifiers: chr9:g.131303393C>A (hg19) ; chr9:g.128541114C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541114C>A , CM000671.2:g.128541114C>A	GRCh38
NC_000009.11:g.131303393C>A , CM000671.1:g.131303393C>A	GRCh37
NC_000009.10:g.130343214C>A	NCBI36
NG_012073.1:g.41423C>A , LRG_484:g.41423C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1112C>A	ENSP00000507095.1:n.*1112C>A
ENST00000683288.1:c.*2040C>A	ENSP00000507477.1:n.*2040C>A
ENST00000683748.1:c.2068C>A	ENSP00000507377.1:p.His690Asn
ENST00000683905.1:c.*717C>A	ENSP00000506960.1:n.*717C>A
ENST00000684139.1:c.1576C>A	ENSP00000507295.1:p.His526Asn
ENST00000684210.1:n.1754C>A
ENST00000684314.1:c.1936C>A	ENSP00000507700.1:p.His646Asn
ENST00000684331.1:c.*761C>A	ENSP00000507431.1:n.*761C>A
ENST00000684463.1:n.679C>A
ENST00000684646.1:c.1828C>A	ENSP00000507723.1:p.His610Asn
ENST00000309971.9:c.2041C>A MANE Select	ENSP00000308622.5:p.His681Asn
ENST00000309971.8:c.2041C>A	ENSP00000308622.4:p.His681Asn
NM_001003722.1:c.2041C>A , LRG_484t1:c.2041C>A	NP_001003722.1:p.His681Asn
XM_006717059.2:c.2077C>A	XP_006717122.1:p.His693Asn
XM_006717060.2:c.2050C>A	XP_006717123.1:p.His684Asn
XM_011518549.1:c.2077C>A	XP_011516851.1:p.His693Asn
XM_011518550.1:c.2077C>A	XP_011516852.1:p.His693Asn
XM_011518551.1:c.2068C>A	XP_011516853.1:p.His690Asn
XM_011518552.1:c.1318C>A	XP_011516854.1:p.His440Asn
XR_242681.3:n.100+2265G>T
XM_006717059.3:c.2077C>A	XP_006717122.1:p.His693Asn
XM_006717060.3:c.2050C>A	XP_006717123.1:p.His684Asn
XM_011518551.2:c.2068C>A	XP_011516853.1:p.His690Asn
XM_024447519.1:c.2050C>A	XP_024303287.1:p.His684Asn
NM_001003722.2:c.2041C>A MANE Select	NP_001003722.1:p.His681Asn