Canonical Allele Identifier: CA2691925820

Gene: GLE1

Linked Data

• gnomAD v4: 9-128541056-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541058_128541059del , CM000671.2:g.128541058_128541059del	GRCh38
NC_000009.11:g.131303337_131303338del , CM000671.1:g.131303337_131303338del	GRCh37
NC_000009.10:g.130343158_130343159del	NCBI36
NG_012073.1:g.41367_41368del , LRG_484:g.41367_41368del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1100-44_*1100-43del	ENSP00000507095.1:n.*1100-44_*1100-43del
ENST00000683288.1:c.*2028-44_*2028-43del	ENSP00000507477.1:n.*2028-44_*2028-43del
ENST00000683748.1:c.2056-44_2056-43del	ENSP00000507377.1:n.2056-44_2056-43del
ENST00000683905.1:c.*705-44_*705-43del	ENSP00000506960.1:n.*705-44_*705-43del
ENST00000684139.1:c.1564-44_1564-43del	ENSP00000507295.1:n.1564-44_1564-43del
ENST00000684210.1:n.1742-44_1742-43del
ENST00000684314.1:c.1924-44_1924-43del	ENSP00000507700.1:n.1924-44_1924-43del
ENST00000684331.1:c.*705_*706del	ENSP00000507431.1:n.*705_*706del
ENST00000684463.1:n.667-44_667-43del
ENST00000684646.1:c.1816-44_1816-43del	ENSP00000507723.1:n.1816-44_1816-43del
ENST00000309971.9:c.2029-44_2029-43del MANE Select	ENSP00000308622.5:n.2029-44_2029-43del
ENST00000309971.8:c.2029-44_2029-43del	ENSP00000308622.4:n.2029-44_2029-43del
NM_001003722.1:c.2029-44_2029-43del , LRG_484t1:c.2029-44_2029-43del	NP_001003722.1:n.2029-44_2029-43del
XM_006717059.2:c.2065-44_2065-43del	XP_006717122.1:n.2065-44_2065-43del
XM_006717060.2:c.2038-44_2038-43del	XP_006717123.1:n.2038-44_2038-43del
XM_011518549.1:c.2065-44_2065-43del	XP_011516851.1:n.2065-44_2065-43del
XM_011518550.1:c.2065-44_2065-43del	XP_011516852.1:n.2065-44_2065-43del
XM_011518551.1:c.2056-44_2056-43del	XP_011516853.1:n.2056-44_2056-43del
XM_011518552.1:c.1306-44_1306-43del	XP_011516854.1:n.1306-44_1306-43del
XR_242681.3:n.100+2321_100+2322del
XR_428600.2:n.36_37del
XM_006717059.3:c.2065-44_2065-43del	XP_006717122.1:n.2065-44_2065-43del
XM_006717060.3:c.2038-44_2038-43del	XP_006717123.1:n.2038-44_2038-43del
XM_011518551.2:c.2056-44_2056-43del	XP_011516853.1:n.2056-44_2056-43del
XM_024447519.1:c.2038-44_2038-43del	XP_024303287.1:n.2038-44_2038-43del
XR_428600.3:n.38_39del
NM_001003722.2:c.2029-44_2029-43del MANE Select	NP_001003722.1:n.2029-44_2029-43del