Canonical Allele Identifier: CA2691925819

Gene: GLE1

Linked Data

• gnomAD v4: 9-128541041-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541042_128541043del , CM000671.2:g.128541042_128541043del	GRCh38
NC_000009.11:g.131303321_131303322del , CM000671.1:g.131303321_131303322del	GRCh37
NC_000009.10:g.130343142_130343143del	NCBI36
NG_012073.1:g.41351_41352del , LRG_484:g.41351_41352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1100-60_*1100-59del	ENSP00000507095.1:n.*1100-60_*1100-59del
ENST00000683288.1:c.*2028-60_*2028-59del	ENSP00000507477.1:n.*2028-60_*2028-59del
ENST00000683748.1:c.2056-60_2056-59del	ENSP00000507377.1:n.2056-60_2056-59del
ENST00000683905.1:c.*705-60_*705-59del	ENSP00000506960.1:n.*705-60_*705-59del
ENST00000684139.1:c.1564-60_1564-59del	ENSP00000507295.1:n.1564-60_1564-59del
ENST00000684210.1:n.1742-60_1742-59del
ENST00000684314.1:c.1924-60_1924-59del	ENSP00000507700.1:n.1924-60_1924-59del
ENST00000684331.1:c.*689_*690del	ENSP00000507431.1:n.*689_*690del
ENST00000684463.1:n.667-60_667-59del
ENST00000684646.1:c.1816-60_1816-59del	ENSP00000507723.1:n.1816-60_1816-59del
ENST00000309971.9:c.2029-60_2029-59del MANE Select	ENSP00000308622.5:n.2029-60_2029-59del
ENST00000309971.8:c.2029-60_2029-59del	ENSP00000308622.4:n.2029-60_2029-59del
NM_001003722.1:c.2029-60_2029-59del , LRG_484t1:c.2029-60_2029-59del	NP_001003722.1:n.2029-60_2029-59del
XM_006717059.2:c.2065-60_2065-59del	XP_006717122.1:n.2065-60_2065-59del
XM_006717060.2:c.2038-60_2038-59del	XP_006717123.1:n.2038-60_2038-59del
XM_011518549.1:c.2065-60_2065-59del	XP_011516851.1:n.2065-60_2065-59del
XM_011518550.1:c.2065-60_2065-59del	XP_011516852.1:n.2065-60_2065-59del
XM_011518551.1:c.2056-60_2056-59del	XP_011516853.1:n.2056-60_2056-59del
XM_011518552.1:c.1306-60_1306-59del	XP_011516854.1:n.1306-60_1306-59del
XR_242681.3:n.100+2336_100+2337del
XR_428600.2:n.51_52del
XM_006717059.3:c.2065-60_2065-59del	XP_006717122.1:n.2065-60_2065-59del
XM_006717060.3:c.2038-60_2038-59del	XP_006717123.1:n.2038-60_2038-59del
XM_011518551.2:c.2056-60_2056-59del	XP_011516853.1:n.2056-60_2056-59del
XM_024447519.1:c.2038-60_2038-59del	XP_024303287.1:n.2038-60_2038-59del
XR_428600.3:n.53_54del
NM_001003722.2:c.2029-60_2029-59del MANE Select	NP_001003722.1:n.2029-60_2029-59del