Canonical Allele Identifier: CA1880333224

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541069_128541073delinsCTCAT , CM000671.2:g.128541069_128541073delinsCTCAT	GRCh38
NC_000009.11:g.131303348_131303352delinsCTCAT , CM000671.1:g.131303348_131303352delinsCTCAT	GRCh37
NC_000009.10:g.130343169_130343173delinsCTCAT	NCBI36
NG_012073.1:g.41378_41382delinsCTCAT , LRG_484:g.41378_41382delinsCTCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1100-33_*1100-29delinsCTCAT	ENSP00000507095.1:n.*1100-33_*1100-29delinsCTCAT
ENST00000683288.1:c.*2028-33_*2028-29delinsCTCAT	ENSP00000507477.1:n.*2028-33_*2028-29delinsCTCAT
ENST00000683748.1:c.2056-33_2056-29delinsCTCAT	ENSP00000507377.1:n.2056-33_2056-29delinsCTCAT
ENST00000683905.1:c.*705-33_*705-29delinsCTCAT	ENSP00000506960.1:n.*705-33_*705-29delinsCTCAT
ENST00000684139.1:c.1564-33_1564-29delinsCTCAT	ENSP00000507295.1:n.1564-33_1564-29delinsCTCAT
ENST00000684210.1:n.1742-33_1742-29delinsCTCAT
ENST00000684314.1:c.1924-33_1924-29delinsCTCAT	ENSP00000507700.1:n.1924-33_1924-29delinsCTCAT
ENST00000684331.1:c.*716_*720delinsCTCAT	ENSP00000507431.1:n.*716_*720delinsCTCAT
ENST00000684463.1:n.667-33_667-29delinsCTCAT
ENST00000684646.1:c.1816-33_1816-29delinsCTCAT	ENSP00000507723.1:n.1816-33_1816-29delinsCTCAT
ENST00000309971.9:c.2029-33_2029-29delinsCTCAT MANE Select	ENSP00000308622.5:n.2029-33_2029-29delinsCTCAT
ENST00000309971.8:c.2029-33_2029-29delinsCTCAT	ENSP00000308622.4:n.2029-33_2029-29delinsCTCAT
NM_001003722.1:c.2029-33_2029-29delinsCTCAT , LRG_484t1:c.2029-33_2029-29delinsCTCAT	NP_001003722.1:n.2029-33_2029-29delinsCTCAT
XM_006717059.2:c.2065-33_2065-29delinsCTCAT	XP_006717122.1:n.2065-33_2065-29delinsCTCAT
XM_006717060.2:c.2038-33_2038-29delinsCTCAT	XP_006717123.1:n.2038-33_2038-29delinsCTCAT
XM_011518549.1:c.2065-33_2065-29delinsCTCAT	XP_011516851.1:n.2065-33_2065-29delinsCTCAT
XM_011518550.1:c.2065-33_2065-29delinsCTCAT	XP_011516852.1:n.2065-33_2065-29delinsCTCAT
XM_011518551.1:c.2056-33_2056-29delinsCTCAT	XP_011516853.1:n.2056-33_2056-29delinsCTCAT
XM_011518552.1:c.1306-33_1306-29delinsCTCAT	XP_011516854.1:n.1306-33_1306-29delinsCTCAT
XR_242681.3:n.100+2306_100+2310delinsATGAG
XR_428600.2:n.21_25delinsATGAG
XM_006717059.3:c.2065-33_2065-29delinsCTCAT	XP_006717122.1:n.2065-33_2065-29delinsCTCAT
XM_006717060.3:c.2038-33_2038-29delinsCTCAT	XP_006717123.1:n.2038-33_2038-29delinsCTCAT
XM_011518551.2:c.2056-33_2056-29delinsCTCAT	XP_011516853.1:n.2056-33_2056-29delinsCTCAT
XM_024447519.1:c.2038-33_2038-29delinsCTCAT	XP_024303287.1:n.2038-33_2038-29delinsCTCAT
XR_428600.3:n.23_27delinsATGAG
NM_001003722.2:c.2029-33_2029-29delinsCTCAT MANE Select	NP_001003722.1:n.2029-33_2029-29delinsCTCAT