Canonical Allele Identifier: CA2502973977
Gene: GLE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128540868_128540869del , CM000671.2:g.128540868_128540869del GRCh38
NC_000009.11:g.131303147_131303148del , CM000671.1:g.131303147_131303148del GRCh37
NC_000009.10:g.130342968_130342969del NCBI36
NG_012073.1:g.41177_41178del , LRG_484:g.41177_41178del

Transcript Alleles

HGVS Amino-acid Change
ENST00000683044.1:c.*1100-234_*1100-233del ENSP00000507095.1:n.*1100-234_*1100-233del
ENST00000683288.1:c.*2028-234_*2028-233del ENSP00000507477.1:n.*2028-234_*2028-233del
ENST00000683748.1:c.2056-234_2056-233del ENSP00000507377.1:n.2056-234_2056-233del
ENST00000683905.1:c.*705-234_*705-233del ENSP00000506960.1:n.*705-234_*705-233del
ENST00000684139.1:c.1564-234_1564-233del ENSP00000507295.1:n.1564-234_1564-233del
ENST00000684210.1:n.1742-234_1742-233del
ENST00000684314.1:c.1924-234_1924-233del ENSP00000507700.1:n.1924-234_1924-233del
ENST00000684331.1:c.*515_*516del ENSP00000507431.1:n.*515_*516del
ENST00000684463.1:n.667-234_667-233del
ENST00000684646.1:c.1816-234_1816-233del ENSP00000507723.1:n.1816-234_1816-233del
ENST00000309971.9:c.2029-234_2029-233del MANE Select ENSP00000308622.5:n.2029-234_2029-233del
ENST00000309971.8:c.2029-234_2029-233del ENSP00000308622.4:n.2029-234_2029-233del
NM_001003722.1:c.2029-234_2029-233del , LRG_484t1:c.2029-234_2029-233del NP_001003722.1:n.2029-234_2029-233del
XM_006717059.2:c.2065-234_2065-233del XP_006717122.1:n.2065-234_2065-233del
XM_006717060.2:c.2038-234_2038-233del XP_006717123.1:n.2038-234_2038-233del
XM_011518549.1:c.2065-234_2065-233del XP_011516851.1:n.2065-234_2065-233del
XM_011518550.1:c.2065-234_2065-233del XP_011516852.1:n.2065-234_2065-233del
XM_011518551.1:c.2056-234_2056-233del XP_011516853.1:n.2056-234_2056-233del
XM_011518552.1:c.1306-234_1306-233del XP_011516854.1:n.1306-234_1306-233del
XR_242681.3:n.100+2511_100+2512del
XR_428600.2:n.124+102_124+103del
XM_006717059.3:c.2065-234_2065-233del XP_006717122.1:n.2065-234_2065-233del
XM_006717060.3:c.2038-234_2038-233del XP_006717123.1:n.2038-234_2038-233del
XM_011518551.2:c.2056-234_2056-233del XP_011516853.1:n.2056-234_2056-233del
XM_024447519.1:c.2038-234_2038-233del XP_024303287.1:n.2038-234_2038-233del
XR_428600.3:n.126+102_126+103del
NM_001003722.2:c.2029-234_2029-233del MANE Select NP_001003722.1:n.2029-234_2029-233del