Canonical Allele Identifier: CA2691925821

Gene: GLE1

Linked Data

• gnomAD v4: 9-128541060-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541061dup , CM000671.2:g.128541061dup	GRCh38
NC_000009.11:g.131303340dup , CM000671.1:g.131303340dup	GRCh37
NC_000009.10:g.130343161dup	NCBI36
NG_012073.1:g.41370dup , LRG_484:g.41370dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1100-41dup	ENSP00000507095.1:n.*1100-41dup
ENST00000683288.1:c.*2028-41dup	ENSP00000507477.1:n.*2028-41dup
ENST00000683748.1:c.2056-41dup	ENSP00000507377.1:n.2056-41dup
ENST00000683905.1:c.*705-41dup	ENSP00000506960.1:n.*705-41dup
ENST00000684139.1:c.1564-41dup	ENSP00000507295.1:n.1564-41dup
ENST00000684210.1:n.1742-41dup
ENST00000684314.1:c.1924-41dup	ENSP00000507700.1:n.1924-41dup
ENST00000684331.1:c.*708dup	ENSP00000507431.1:n.*708dup
ENST00000684463.1:n.667-41dup
ENST00000684646.1:c.1816-41dup	ENSP00000507723.1:n.1816-41dup
ENST00000309971.9:c.2029-41dup MANE Select	ENSP00000308622.5:n.2029-41dup
ENST00000309971.8:c.2029-41dup	ENSP00000308622.4:n.2029-41dup
NM_001003722.1:c.2029-41dup , LRG_484t1:c.2029-41dup	NP_001003722.1:n.2029-41dup
XM_006717059.2:c.2065-41dup	XP_006717122.1:n.2065-41dup
XM_006717060.2:c.2038-41dup	XP_006717123.1:n.2038-41dup
XM_011518549.1:c.2065-41dup	XP_011516851.1:n.2065-41dup
XM_011518550.1:c.2065-41dup	XP_011516852.1:n.2065-41dup
XM_011518551.1:c.2056-41dup	XP_011516853.1:n.2056-41dup
XM_011518552.1:c.1306-41dup	XP_011516854.1:n.1306-41dup
XR_242681.3:n.100+2318dup
XR_428600.2:n.33dup
XM_006717059.3:c.2065-41dup	XP_006717122.1:n.2065-41dup
XM_006717060.3:c.2038-41dup	XP_006717123.1:n.2038-41dup
XM_011518551.2:c.2056-41dup	XP_011516853.1:n.2056-41dup
XM_024447519.1:c.2038-41dup	XP_024303287.1:n.2038-41dup
XR_428600.3:n.35dup
NM_001003722.2:c.2029-41dup MANE Select	NP_001003722.1:n.2029-41dup