Canonical Allele Identifier: CA375046421

Gene: GLE1

Linked Data

• gnomAD v4: 9-128541153-T-A
• MyVariant Identifiers: chr9:g.131303432T>A (hg19) ; chr9:g.128541153T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541153T>A , CM000671.2:g.128541153T>A	GRCh38
NC_000009.11:g.131303432T>A , CM000671.1:g.131303432T>A	GRCh37
NC_000009.10:g.130343253T>A	NCBI36
NG_012073.1:g.41462T>A , LRG_484:g.41462T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1151T>A	ENSP00000507095.1:n.*1151T>A
ENST00000683288.1:c.*2079T>A	ENSP00000507477.1:n.*2079T>A
ENST00000683748.1:c.2107T>A	ENSP00000507377.1:p.Ser703Thr
ENST00000683905.1:c.*756T>A	ENSP00000506960.1:n.*756T>A
ENST00000684139.1:c.1615T>A	ENSP00000507295.1:p.Ser539Thr
ENST00000684210.1:n.1793T>A
ENST00000684314.1:c.1975T>A	ENSP00000507700.1:p.Ser659Thr
ENST00000684331.1:c.*800T>A	ENSP00000507431.1:n.*800T>A
ENST00000684463.1:n.718T>A
ENST00000684646.1:c.1867T>A	ENSP00000507723.1:p.Ser623Thr
ENST00000309971.9:c.2080T>A MANE Select	ENSP00000308622.5:p.Ser694Thr
ENST00000309971.8:c.2080T>A	ENSP00000308622.4:p.Ser694Thr
NM_001003722.1:c.2080T>A , LRG_484t1:c.2080T>A	NP_001003722.1:p.Ser694Thr
XM_006717059.2:c.2116T>A	XP_006717122.1:p.Ser706Thr
XM_006717060.2:c.2089T>A	XP_006717123.1:p.Ser697Thr
XM_011518549.1:c.2116T>A	XP_011516851.1:p.Ser706Thr
XM_011518550.1:c.2116T>A	XP_011516852.1:p.Ser706Thr
XM_011518551.1:c.2107T>A	XP_011516853.1:p.Ser703Thr
XM_011518552.1:c.1357T>A	XP_011516854.1:p.Ser453Thr
XR_242681.3:n.100+2226A>T
XM_006717059.3:c.2116T>A	XP_006717122.1:p.Ser706Thr
XM_006717060.3:c.2089T>A	XP_006717123.1:p.Ser697Thr
XM_011518551.2:c.2107T>A	XP_011516853.1:p.Ser703Thr
XM_024447519.1:c.2089T>A	XP_024303287.1:p.Ser697Thr
NM_001003722.2:c.2080T>A MANE Select	NP_001003722.1:p.Ser694Thr