Canonical Allele Identifier: CA1880332915

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540748_128540749delinsAG , CM000671.2:g.128540748_128540749delinsAG	GRCh38
NC_000009.11:g.131303027_131303028delinsAG , CM000671.1:g.131303027_131303028delinsAG	GRCh37
NC_000009.10:g.130342848_130342849delinsAG	NCBI36
NG_012073.1:g.41057_41058delinsAG , LRG_484:g.41057_41058delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1100-354_*1100-353delinsAG	ENSP00000507095.1:n.*1100-354_*1100-353delinsAG
ENST00000683288.1:c.*2028-354_*2028-353delinsAG	ENSP00000507477.1:n.*2028-354_*2028-353delinsAG
ENST00000683748.1:c.2056-354_2056-353delinsAG	ENSP00000507377.1:n.2056-354_2056-353delinsAG
ENST00000683905.1:c.*705-354_*705-353delinsAG	ENSP00000506960.1:n.*705-354_*705-353delinsAG
ENST00000684139.1:c.1564-354_1564-353delinsAG	ENSP00000507295.1:n.1564-354_1564-353delinsAG
ENST00000684210.1:n.1742-354_1742-353delinsAG
ENST00000684314.1:c.1924-354_1924-353delinsAG	ENSP00000507700.1:n.1924-354_1924-353delinsAG
ENST00000684331.1:c.*395_*396delinsAG	ENSP00000507431.1:n.*395_*396delinsAG
ENST00000684463.1:n.667-354_667-353delinsAG
ENST00000684646.1:c.1816-354_1816-353delinsAG	ENSP00000507723.1:n.1816-354_1816-353delinsAG
ENST00000309971.9:c.2029-354_2029-353delinsAG MANE Select	ENSP00000308622.5:n.2029-354_2029-353delinsAG
ENST00000309971.8:c.2029-354_2029-353delinsAG	ENSP00000308622.4:n.2029-354_2029-353delinsAG
NM_001003722.1:c.2029-354_2029-353delinsAG , LRG_484t1:c.2029-354_2029-353delinsAG	NP_001003722.1:n.2029-354_2029-353delinsAG
XM_006717059.2:c.2065-354_2065-353delinsAG	XP_006717122.1:n.2065-354_2065-353delinsAG
XM_006717060.2:c.2038-354_2038-353delinsAG	XP_006717123.1:n.2038-354_2038-353delinsAG
XM_011518549.1:c.2065-354_2065-353delinsAG	XP_011516851.1:n.2065-354_2065-353delinsAG
XM_011518550.1:c.2065-354_2065-353delinsAG	XP_011516852.1:n.2065-354_2065-353delinsAG
XM_011518551.1:c.2056-354_2056-353delinsAG	XP_011516853.1:n.2056-354_2056-353delinsAG
XM_011518552.1:c.1306-354_1306-353delinsAG	XP_011516854.1:n.1306-354_1306-353delinsAG
XR_242681.3:n.100+2630_100+2631delinsCT
XR_428600.2:n.124+221_124+222delinsCT
XM_006717059.3:c.2065-354_2065-353delinsAG	XP_006717122.1:n.2065-354_2065-353delinsAG
XM_006717060.3:c.2038-354_2038-353delinsAG	XP_006717123.1:n.2038-354_2038-353delinsAG
XM_011518551.2:c.2056-354_2056-353delinsAG	XP_011516853.1:n.2056-354_2056-353delinsAG
XM_024447519.1:c.2038-354_2038-353delinsAG	XP_024303287.1:n.2038-354_2038-353delinsAG
XR_428600.3:n.126+221_126+222delinsCT
NM_001003722.2:c.2029-354_2029-353delinsAG MANE Select	NP_001003722.1:n.2029-354_2029-353delinsAG