Canonical Allele Identifier: CA375046236

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131302591T>A (hg19) ; chr9:g.128540312T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540312T>A , CM000671.2:g.128540312T>A	GRCh38
NC_000009.11:g.131302591T>A , CM000671.1:g.131302591T>A	GRCh37
NC_000009.10:g.130342412T>A	NCBI36
NG_012073.1:g.40621T>A , LRG_484:g.40621T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1073T>A	ENSP00000507095.1:n.*1073T>A
ENST00000683288.1:c.*2001T>A	ENSP00000507477.1:n.*2001T>A
ENST00000683748.1:c.2029T>A	ENSP00000507377.1:p.Phe677Ile
ENST00000683905.1:c.*678T>A	ENSP00000506960.1:n.*678T>A
ENST00000684139.1:c.1537T>A	ENSP00000507295.1:p.Phe513Ile
ENST00000684210.1:n.1715T>A
ENST00000684314.1:c.1897T>A	ENSP00000507700.1:p.Phe633Ile
ENST00000684331.1:c.2002T>A	ENSP00000507431.1:p.Phe668Ile
ENST00000684463.1:n.640T>A
ENST00000684646.1:c.1789T>A	ENSP00000507723.1:p.Phe597Ile
ENST00000309971.9:c.2002T>A MANE Select	ENSP00000308622.5:p.Phe668Ile
ENST00000309971.8:c.2002T>A	ENSP00000308622.4:p.Phe668Ile
NM_001003722.1:c.2002T>A , LRG_484t1:c.2002T>A	NP_001003722.1:p.Phe668Ile
XM_006717059.2:c.2038T>A	XP_006717122.1:p.Phe680Ile
XM_006717060.2:c.2011T>A	XP_006717123.1:p.Phe671Ile
XM_011518549.1:c.2038T>A	XP_011516851.1:p.Phe680Ile
XM_011518550.1:c.2038T>A	XP_011516852.1:p.Phe680Ile
XM_011518551.1:c.2029T>A	XP_011516853.1:p.Phe677Ile
XM_011518552.1:c.1279T>A	XP_011516854.1:p.Phe427Ile
XR_242681.3:n.100+3067A>T
XR_428600.2:n.124+658A>T
XM_006717059.3:c.2038T>A	XP_006717122.1:p.Phe680Ile
XM_006717060.3:c.2011T>A	XP_006717123.1:p.Phe671Ile
XM_011518551.2:c.2029T>A	XP_011516853.1:p.Phe677Ile
XM_024447519.1:c.2011T>A	XP_024303287.1:p.Phe671Ile
XR_428600.3:n.126+658A>T
NM_001003722.2:c.2002T>A MANE Select	NP_001003722.1:p.Phe668Ile