Canonical Allele Identifier: CA2691925663

Gene: GLE1

Linked Data

• gnomAD v4: 9-128540353-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540353G>T , CM000671.2:g.128540353G>T	GRCh38
NC_000009.11:g.131302632G>T , CM000671.1:g.131302632G>T	GRCh37
NC_000009.10:g.130342453G>T	NCBI36
NG_012073.1:g.40662G>T , LRG_484:g.40662G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1099+15G>T	ENSP00000507095.1:n.*1099+15G>T
ENST00000683288.1:c.*2027+15G>T	ENSP00000507477.1:n.*2027+15G>T
ENST00000683748.1:c.2055+15G>T	ENSP00000507377.1:n.2055+15G>T
ENST00000683905.1:c.*704+15G>T	ENSP00000506960.1:n.*704+15G>T
ENST00000684139.1:c.1563+15G>T	ENSP00000507295.1:n.1563+15G>T
ENST00000684210.1:n.1741+15G>T
ENST00000684314.1:c.1923+15G>T	ENSP00000507700.1:n.1923+15G>T
ENST00000684331.1:c.2043G>T	ENSP00000507431.1:p.Ter681Tyr
ENST00000684463.1:n.666+15G>T
ENST00000684646.1:c.1815+15G>T	ENSP00000507723.1:n.1815+15G>T
ENST00000309971.9:c.2028+15G>T MANE Select	ENSP00000308622.5:n.2028+15G>T
ENST00000309971.8:c.2028+15G>T	ENSP00000308622.4:n.2028+15G>T
NM_001003722.1:c.2028+15G>T , LRG_484t1:c.2028+15G>T	NP_001003722.1:n.2028+15G>T
XM_006717059.2:c.2064+15G>T	XP_006717122.1:n.2064+15G>T
XM_006717060.2:c.2037+15G>T	XP_006717123.1:n.2037+15G>T
XM_011518549.1:c.2064+15G>T	XP_011516851.1:n.2064+15G>T
XM_011518550.1:c.2064+15G>T	XP_011516852.1:n.2064+15G>T
XM_011518551.1:c.2055+15G>T	XP_011516853.1:n.2055+15G>T
XM_011518552.1:c.1305+15G>T	XP_011516854.1:n.1305+15G>T
XR_242681.3:n.100+3026C>A
XR_428600.2:n.124+617C>A
XM_006717059.3:c.2064+15G>T	XP_006717122.1:n.2064+15G>T
XM_006717060.3:c.2037+15G>T	XP_006717123.1:n.2037+15G>T
XM_011518551.2:c.2055+15G>T	XP_011516853.1:n.2055+15G>T
XM_024447519.1:c.2037+15G>T	XP_024303287.1:n.2037+15G>T
XR_428600.3:n.126+617C>A
NM_001003722.2:c.2028+15G>T MANE Select	NP_001003722.1:n.2028+15G>T