Canonical Allele Identifier: CA467288875

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131303434C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541155C>G , CM000671.2:g.128541155C>G	GRCh38
NC_000009.11:g.131303434C>G , CM000671.1:g.131303434C>G	GRCh37
NC_000009.10:g.130343255C>G	NCBI36
NG_012073.1:g.41464C>G , LRG_484:g.41464C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1153C>G	ENSP00000507095.1:n.*1153C>G
ENST00000683288.1:c.*2081C>G	ENSP00000507477.1:n.*2081C>G
ENST00000683748.1:c.2109C>G	ENSP00000507377.1:p.Ser703=
ENST00000683905.1:c.*758C>G	ENSP00000506960.1:n.*758C>G
ENST00000684139.1:c.1617C>G	ENSP00000507295.1:p.Ser539=
ENST00000684210.1:n.1795C>G
ENST00000684314.1:c.1977C>G	ENSP00000507700.1:p.Ser659=
ENST00000684331.1:c.*802C>G	ENSP00000507431.1:n.*802C>G
ENST00000684463.1:n.720C>G
ENST00000684646.1:c.1869C>G	ENSP00000507723.1:p.Ser623=
ENST00000309971.9:c.2082C>G MANE Select	ENSP00000308622.5:p.Ser694=
ENST00000309971.8:c.2082C>G	ENSP00000308622.4:p.Ser694=
NM_001003722.1:c.2082C>G , LRG_484t1:c.2082C>G	NP_001003722.1:p.Ser694=
XM_006717059.2:c.2118C>G	XP_006717122.1:p.Ser706=
XM_006717060.2:c.2091C>G	XP_006717123.1:p.Ser697=
XM_011518549.1:c.2118C>G	XP_011516851.1:p.Ser706=
XM_011518550.1:c.2118C>G	XP_011516852.1:p.Ser706=
XM_011518551.1:c.2109C>G	XP_011516853.1:p.Ser703=
XM_011518552.1:c.1359C>G	XP_011516854.1:p.Ser453=
XR_242681.3:n.100+2224G>C
XM_006717059.3:c.2118C>G	XP_006717122.1:p.Ser706=
XM_006717060.3:c.2091C>G	XP_006717123.1:p.Ser697=
XM_011518551.2:c.2109C>G	XP_011516853.1:p.Ser703=
XM_024447519.1:c.2091C>G	XP_024303287.1:p.Ser697=
NM_001003722.2:c.2082C>G MANE Select	NP_001003722.1:p.Ser694=