Canonical Allele Identifier: CA467286696

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131302554A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540275A>G , CM000671.2:g.128540275A>G	GRCh38
NC_000009.11:g.131302554A>G , CM000671.1:g.131302554A>G	GRCh37
NC_000009.10:g.130342375A>G	NCBI36
NG_012073.1:g.40584A>G , LRG_484:g.40584A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1036A>G	ENSP00000507095.1:n.*1036A>G
ENST00000683288.1:c.*1964A>G	ENSP00000507477.1:n.*1964A>G
ENST00000683748.1:c.1992A>G	ENSP00000507377.1:p.Arg664=
ENST00000683905.1:c.*641A>G	ENSP00000506960.1:n.*641A>G
ENST00000684139.1:c.1500A>G	ENSP00000507295.1:p.Arg500=
ENST00000684210.1:n.1678A>G
ENST00000684314.1:c.1860A>G	ENSP00000507700.1:p.Arg620=
ENST00000684331.1:c.1965A>G	ENSP00000507431.1:p.Arg655=
ENST00000684463.1:n.603A>G
ENST00000684646.1:c.1752A>G	ENSP00000507723.1:p.Arg584=
ENST00000309971.9:c.1965A>G MANE Select	ENSP00000308622.5:p.Arg655=
ENST00000309971.8:c.1965A>G	ENSP00000308622.4:p.Arg655=
NM_001003722.1:c.1965A>G , LRG_484t1:c.1965A>G	NP_001003722.1:p.Arg655=
XM_006717059.2:c.2001A>G	XP_006717122.1:p.Arg667=
XM_006717060.2:c.1974A>G	XP_006717123.1:p.Arg658=
XM_011518549.1:c.2001A>G	XP_011516851.1:p.Arg667=
XM_011518550.1:c.2001A>G	XP_011516852.1:p.Arg667=
XM_011518551.1:c.1992A>G	XP_011516853.1:p.Arg664=
XM_011518552.1:c.1242A>G	XP_011516854.1:p.Arg414=
XR_242681.3:n.100+3104T>C
XR_428600.2:n.124+695T>C
XM_006717059.3:c.2001A>G	XP_006717122.1:p.Arg667=
XM_006717060.3:c.1974A>G	XP_006717123.1:p.Arg658=
XM_011518551.2:c.1992A>G	XP_011516853.1:p.Arg664=
XM_024447519.1:c.1974A>G	XP_024303287.1:p.Arg658=
XR_428600.3:n.126+695T>C
NM_001003722.2:c.1965A>G MANE Select	NP_001003722.1:p.Arg655=