Canonical Allele Identifier: CA860266329

Gene: GLE1

Linked Data

• dbSNP Id: rs1201045174
• gnomAD v3: 9-128540217-T-A
• gnomAD v4: 9-128540217-T-A
• MyVariant Identifiers: chr9:g.131302496T>A (hg19) ; chr9:g.128540217T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540217T>A , CM000671.2:g.128540217T>A	GRCh38
NC_000009.11:g.131302496T>A , CM000671.1:g.131302496T>A	GRCh37
NC_000009.10:g.130342317T>A	NCBI36
NG_012073.1:g.40526T>A , LRG_484:g.40526T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1036-58T>A	ENSP00000507095.1:n.*1036-58T>A
ENST00000683288.1:c.*1964-58T>A	ENSP00000507477.1:n.*1964-58T>A
ENST00000683748.1:c.1992-58T>A	ENSP00000507377.1:n.1992-58T>A
ENST00000683905.1:c.*641-58T>A	ENSP00000506960.1:n.*641-58T>A
ENST00000684139.1:c.1500-58T>A	ENSP00000507295.1:n.1500-58T>A
ENST00000684210.1:n.1678-58T>A
ENST00000684314.1:c.1860-58T>A	ENSP00000507700.1:n.1860-58T>A
ENST00000684331.1:c.1965-58T>A	ENSP00000507431.1:n.1965-58T>A
ENST00000684463.1:n.603-58T>A
ENST00000684646.1:c.1752-58T>A	ENSP00000507723.1:n.1752-58T>A
ENST00000309971.9:c.1965-58T>A MANE Select	ENSP00000308622.5:n.1965-58T>A
ENST00000309971.8:c.1965-58T>A	ENSP00000308622.4:n.1965-58T>A
NM_001003722.1:c.1965-58T>A , LRG_484t1:c.1965-58T>A	NP_001003722.1:n.1965-58T>A
XM_006717059.2:c.2001-58T>A	XP_006717122.1:n.2001-58T>A
XM_006717060.2:c.1974-58T>A	XP_006717123.1:n.1974-58T>A
XM_011518549.1:c.2001-58T>A	XP_011516851.1:n.2001-58T>A
XM_011518550.1:c.2001-58T>A	XP_011516852.1:n.2001-58T>A
XM_011518551.1:c.1992-58T>A	XP_011516853.1:n.1992-58T>A
XM_011518552.1:c.1242-58T>A	XP_011516854.1:n.1242-58T>A
XR_242681.3:n.100+3162A>T
XR_428600.2:n.124+753A>T
XM_006717059.3:c.2001-58T>A	XP_006717122.1:n.2001-58T>A
XM_006717060.3:c.1974-58T>A	XP_006717123.1:n.1974-58T>A
XM_011518551.2:c.1992-58T>A	XP_011516853.1:n.1992-58T>A
XM_024447519.1:c.1974-58T>A	XP_024303287.1:n.1974-58T>A
XR_428600.3:n.126+753A>T
NM_001003722.2:c.1965-58T>A MANE Select	NP_001003722.1:n.1965-58T>A