Canonical Allele Identifier: CA1880333182

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541026_128541029delinsGCTT , CM000671.2:g.128541026_128541029delinsGCTT	GRCh38
NC_000009.11:g.131303305_131303308delinsGCTT , CM000671.1:g.131303305_131303308delinsGCTT	GRCh37
NC_000009.10:g.130343126_130343129delinsGCTT	NCBI36
NG_012073.1:g.41335_41338delinsGCTT , LRG_484:g.41335_41338delinsGCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000683044.1:c.*1100-76_*1100-73delinsGCTT	ENSP00000507095.1:n.*1100-76_*1100-73deli...
ENST00000683288.1:c.*2028-76_*2028-73delinsGCTT	ENSP00000507477.1:n.*2028-76_*2028-73deli...
ENST00000683748.1:c.2056-76_2056-73delinsGCTT	ENSP00000507377.1:n.2056-76_2056-73delins...
ENST00000683905.1:c.*705-76_*705-73delinsGCTT	ENSP00000506960.1:n.*705-76_*705-73delins...
ENST00000684139.1:c.1564-76_1564-73delinsGCTT	ENSP00000507295.1:n.1564-76_1564-73delins...
ENST00000684210.1:n.1742-76_1742-73delinsGCTT
ENST00000684314.1:c.1924-76_1924-73delinsGCTT	ENSP00000507700.1:n.1924-76_1924-73delins...
ENST00000684331.1:c.*673_*676delinsGCTT	ENSP00000507431.1:n.*673_*676delinsGCTT
ENST00000684463.1:n.667-76_667-73delinsGCTT
ENST00000684646.1:c.1816-76_1816-73delinsGCTT	ENSP00000507723.1:n.1816-76_1816-73delins...
ENST00000309971.9:c.2029-76_2029-73delinsGCTT MANE Select	ENSP00000308622.5:n.2029-76_2029-73delins...
ENST00000309971.8:c.2029-76_2029-73delinsGCTT	ENSP00000308622.4:n.2029-76_2029-73delins...
NM_001003722.1:c.2029-76_2029-73delinsGCTT , LRG_484t1:c.2029-76_2029-73delinsGCTT	NP_001003722.1:n.2029-76_2029-73delinsGCT...
XM_006717059.2:c.2065-76_2065-73delinsGCTT	XP_006717122.1:n.2065-76_2065-73delinsGCT...
XM_006717060.2:c.2038-76_2038-73delinsGCTT	XP_006717123.1:n.2038-76_2038-73delinsGCT...
XM_011518549.1:c.2065-76_2065-73delinsGCTT	XP_011516851.1:n.2065-76_2065-73delinsGCT...
XM_011518550.1:c.2065-76_2065-73delinsGCTT	XP_011516852.1:n.2065-76_2065-73delinsGCT...
XM_011518551.1:c.2056-76_2056-73delinsGCTT	XP_011516853.1:n.2056-76_2056-73delinsGCT...
XM_011518552.1:c.1306-76_1306-73delinsGCTT	XP_011516854.1:n.1306-76_1306-73delinsGCT...
XR_242681.3:n.100+2350_100+2353delinsAAGC
XR_428600.2:n.65_68delinsAAGC
XM_006717059.3:c.2065-76_2065-73delinsGCTT	XP_006717122.1:n.2065-76_2065-73delinsGCT...
XM_006717060.3:c.2038-76_2038-73delinsGCTT	XP_006717123.1:n.2038-76_2038-73delinsGCT...
XM_011518551.2:c.2056-76_2056-73delinsGCTT	XP_011516853.1:n.2056-76_2056-73delinsGCT...
XM_024447519.1:c.2038-76_2038-73delinsGCTT	XP_024303287.1:n.2038-76_2038-73delinsGCT...
XR_428600.3:n.67_70delinsAAGC
NM_001003722.2:c.2029-76_2029-73delinsGCTT MANE Select	NP_001003722.1:n.2029-76_2029-73delinsGCT...