Canonical Allele Identifier: CA375046372

Gene: GLE1

Linked Data

• gnomAD v4: 9-128541129-G-A
• MyVariant Identifiers: chr9:g.131303408G>A (hg19) ; chr9:g.128541129G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541129G>A , CM000671.2:g.128541129G>A	GRCh38
NC_000009.11:g.131303408G>A , CM000671.1:g.131303408G>A	GRCh37
NC_000009.10:g.130343229G>A	NCBI36
NG_012073.1:g.41438G>A , LRG_484:g.41438G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000683044.1:c.*1127G>A	ENSP00000507095.1:n.*1127G>A
ENST00000683288.1:c.*2055G>A	ENSP00000507477.1:n.*2055G>A
ENST00000683748.1:c.2083G>A	ENSP00000507377.1:p.Val695Ile
ENST00000683905.1:c.*732G>A	ENSP00000506960.1:n.*732G>A
ENST00000684139.1:c.1591G>A	ENSP00000507295.1:p.Val531Ile
ENST00000684210.1:n.1769G>A
ENST00000684314.1:c.1951G>A	ENSP00000507700.1:p.Val651Ile
ENST00000684331.1:c.*776G>A	ENSP00000507431.1:n.*776G>A
ENST00000684463.1:n.694G>A
ENST00000684646.1:c.1843G>A	ENSP00000507723.1:p.Val615Ile
ENST00000309971.9:c.2056G>A MANE Select	ENSP00000308622.5:p.Val686Ile
ENST00000309971.8:c.2056G>A	ENSP00000308622.4:p.Val686Ile
NM_001003722.1:c.2056G>A , LRG_484t1:c.2056G>A	NP_001003722.1:p.Val686Ile
XM_006717059.2:c.2092G>A	XP_006717122.1:p.Val698Ile
XM_006717060.2:c.2065G>A	XP_006717123.1:p.Val689Ile
XM_011518549.1:c.2092G>A	XP_011516851.1:p.Val698Ile
XM_011518550.1:c.2092G>A	XP_011516852.1:p.Val698Ile
XM_011518551.1:c.2083G>A	XP_011516853.1:p.Val695Ile
XM_011518552.1:c.1333G>A	XP_011516854.1:p.Val445Ile
XR_242681.3:n.100+2250C>T
XM_006717059.3:c.2092G>A	XP_006717122.1:p.Val698Ile
XM_006717060.3:c.2065G>A	XP_006717123.1:p.Val689Ile
XM_011518551.2:c.2083G>A	XP_011516853.1:p.Val695Ile
XM_024447519.1:c.2065G>A	XP_024303287.1:p.Val689Ile
NM_001003722.2:c.2056G>A MANE Select	NP_001003722.1:p.Val686Ile