Canonical Allele Identifier: CA1880333089

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540891_128540894delinsGAAT , CM000671.2:g.128540891_128540894delinsGAAT	GRCh38
NC_000009.11:g.131303170_131303173delinsGAAT , CM000671.1:g.131303170_131303173delinsGAAT	GRCh37
NC_000009.10:g.130342991_130342994delinsGAAT	NCBI36
NG_012073.1:g.41200_41203delinsGAAT , LRG_484:g.41200_41203delinsGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1100-211_*1100-208delinsGAAT	ENSP00000507095.1:n.*1100-211_*1100-208delinsGAAT
ENST00000683288.1:c.*2028-211_*2028-208delinsGAAT	ENSP00000507477.1:n.*2028-211_*2028-208delinsGAAT
ENST00000683748.1:c.2056-211_2056-208delinsGAAT	ENSP00000507377.1:n.2056-211_2056-208delinsGAAT
ENST00000683905.1:c.*705-211_*705-208delinsGAAT	ENSP00000506960.1:n.*705-211_*705-208delinsGAAT
ENST00000684139.1:c.1564-211_1564-208delinsGAAT	ENSP00000507295.1:n.1564-211_1564-208delinsGAAT
ENST00000684210.1:n.1742-211_1742-208delinsGAAT
ENST00000684314.1:c.1924-211_1924-208delinsGAAT	ENSP00000507700.1:n.1924-211_1924-208delinsGAAT
ENST00000684331.1:c.*538_*541delinsGAAT	ENSP00000507431.1:n.*538_*541delinsGAAT
ENST00000684463.1:n.667-211_667-208delinsGAAT
ENST00000684646.1:c.1816-211_1816-208delinsGAAT	ENSP00000507723.1:n.1816-211_1816-208delinsGAAT
ENST00000309971.9:c.2029-211_2029-208delinsGAAT MANE Select	ENSP00000308622.5:n.2029-211_2029-208delinsGAAT
ENST00000309971.8:c.2029-211_2029-208delinsGAAT	ENSP00000308622.4:n.2029-211_2029-208delinsGAAT
NM_001003722.1:c.2029-211_2029-208delinsGAAT , LRG_484t1:c.2029-211_2029-208delinsGAAT	NP_001003722.1:n.2029-211_2029-208delinsGAAT
XM_006717059.2:c.2065-211_2065-208delinsGAAT	XP_006717122.1:n.2065-211_2065-208delinsGAAT
XM_006717060.2:c.2038-211_2038-208delinsGAAT	XP_006717123.1:n.2038-211_2038-208delinsGAAT
XM_011518549.1:c.2065-211_2065-208delinsGAAT	XP_011516851.1:n.2065-211_2065-208delinsGAAT
XM_011518550.1:c.2065-211_2065-208delinsGAAT	XP_011516852.1:n.2065-211_2065-208delinsGAAT
XM_011518551.1:c.2056-211_2056-208delinsGAAT	XP_011516853.1:n.2056-211_2056-208delinsGAAT
XM_011518552.1:c.1306-211_1306-208delinsGAAT	XP_011516854.1:n.1306-211_1306-208delinsGAAT
XR_242681.3:n.100+2485_100+2488delinsATTC
XR_428600.2:n.124+76_124+79delinsATTC
XM_006717059.3:c.2065-211_2065-208delinsGAAT	XP_006717122.1:n.2065-211_2065-208delinsGAAT
XM_006717060.3:c.2038-211_2038-208delinsGAAT	XP_006717123.1:n.2038-211_2038-208delinsGAAT
XM_011518551.2:c.2056-211_2056-208delinsGAAT	XP_011516853.1:n.2056-211_2056-208delinsGAAT
XM_024447519.1:c.2038-211_2038-208delinsGAAT	XP_024303287.1:n.2038-211_2038-208delinsGAAT
XR_428600.3:n.126+76_126+79delinsATTC
NM_001003722.2:c.2029-211_2029-208delinsGAAT MANE Select	NP_001003722.1:n.2029-211_2029-208delinsGAAT