Canonical Allele Identifier: CA375046132

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131302564A>G (hg19) ; chr9:g.128540285A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540285A>G , CM000671.2:g.128540285A>G	GRCh38
NC_000009.11:g.131302564A>G , CM000671.1:g.131302564A>G	GRCh37
NC_000009.10:g.130342385A>G	NCBI36
NG_012073.1:g.40594A>G , LRG_484:g.40594A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1046A>G	ENSP00000507095.1:n.*1046A>G
ENST00000683288.1:c.*1974A>G	ENSP00000507477.1:n.*1974A>G
ENST00000683748.1:c.2002A>G	ENSP00000507377.1:p.Ile668Val
ENST00000683905.1:c.*651A>G	ENSP00000506960.1:n.*651A>G
ENST00000684139.1:c.1510A>G	ENSP00000507295.1:p.Ile504Val
ENST00000684210.1:n.1688A>G
ENST00000684314.1:c.1870A>G	ENSP00000507700.1:p.Ile624Val
ENST00000684331.1:c.1975A>G	ENSP00000507431.1:p.Ile659Val
ENST00000684463.1:n.613A>G
ENST00000684646.1:c.1762A>G	ENSP00000507723.1:p.Ile588Val
ENST00000309971.9:c.1975A>G MANE Select	ENSP00000308622.5:p.Ile659Val
ENST00000309971.8:c.1975A>G	ENSP00000308622.4:p.Ile659Val
NM_001003722.1:c.1975A>G , LRG_484t1:c.1975A>G	NP_001003722.1:p.Ile659Val
XM_006717059.2:c.2011A>G	XP_006717122.1:p.Ile671Val
XM_006717060.2:c.1984A>G	XP_006717123.1:p.Ile662Val
XM_011518549.1:c.2011A>G	XP_011516851.1:p.Ile671Val
XM_011518550.1:c.2011A>G	XP_011516852.1:p.Ile671Val
XM_011518551.1:c.2002A>G	XP_011516853.1:p.Ile668Val
XM_011518552.1:c.1252A>G	XP_011516854.1:p.Ile418Val
XR_242681.3:n.100+3094T>C
XR_428600.2:n.124+685T>C
XM_006717059.3:c.2011A>G	XP_006717122.1:p.Ile671Val
XM_006717060.3:c.1984A>G	XP_006717123.1:p.Ile662Val
XM_011518551.2:c.2002A>G	XP_011516853.1:p.Ile668Val
XM_024447519.1:c.1984A>G	XP_024303287.1:p.Ile662Val
XR_428600.3:n.126+685T>C
NM_001003722.2:c.1975A>G MANE Select	NP_001003722.1:p.Ile659Val