Canonical Allele Identifier: CA1129340019

Gene: GLE1

Linked Data

• dbSNP Id: rs1847859098
• gnomAD v3: 9-128540640-T-TA
• gnomAD v4: 9-128540640-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540641dup , CM000671.2:g.128540641dup	GRCh38
NC_000009.11:g.131302920dup , CM000671.1:g.131302920dup	GRCh37
NC_000009.10:g.130342741dup	NCBI36
NG_012073.1:g.40950dup , LRG_484:g.40950dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1099+303dup	ENSP00000507095.1:n.*1099+303dup
ENST00000683288.1:c.*2027+303dup	ENSP00000507477.1:n.*2027+303dup
ENST00000683748.1:c.2055+303dup	ENSP00000507377.1:n.2055+303dup
ENST00000683905.1:c.*704+303dup	ENSP00000506960.1:n.*704+303dup
ENST00000684139.1:c.1563+303dup	ENSP00000507295.1:n.1563+303dup
ENST00000684210.1:n.1741+303dup
ENST00000684314.1:c.1923+303dup	ENSP00000507700.1:n.1923+303dup
ENST00000684331.1:c.*288dup	ENSP00000507431.1:n.*288dup
ENST00000684463.1:n.666+303dup
ENST00000684646.1:c.1815+303dup	ENSP00000507723.1:n.1815+303dup
ENST00000309971.9:c.2028+303dup MANE Select	ENSP00000308622.5:n.2028+303dup
ENST00000309971.8:c.2028+303dup	ENSP00000308622.4:n.2028+303dup
NM_001003722.1:c.2028+303dup , LRG_484t1:c.2028+303dup	NP_001003722.1:n.2028+303dup
XM_006717059.2:c.2064+303dup	XP_006717122.1:n.2064+303dup
XM_006717060.2:c.2037+303dup	XP_006717123.1:n.2037+303dup
XM_011518549.1:c.2064+303dup	XP_011516851.1:n.2064+303dup
XM_011518550.1:c.2064+303dup	XP_011516852.1:n.2064+303dup
XM_011518551.1:c.2055+303dup	XP_011516853.1:n.2055+303dup
XM_011518552.1:c.1305+303dup	XP_011516854.1:n.1305+303dup
XR_242681.3:n.100+2738dup
XR_428600.2:n.124+329dup
XM_006717059.3:c.2064+303dup	XP_006717122.1:n.2064+303dup
XM_006717060.3:c.2037+303dup	XP_006717123.1:n.2037+303dup
XM_011518551.2:c.2055+303dup	XP_011516853.1:n.2055+303dup
XM_024447519.1:c.2037+303dup	XP_024303287.1:n.2037+303dup
XR_428600.3:n.126+329dup
NM_001003722.2:c.2028+303dup MANE Select	NP_001003722.1:n.2028+303dup