Canonical Allele Identifier: CA1880333231

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541073_128541075delinsTTC , CM000671.2:g.128541073_128541075delinsTTC	GRCh38
NC_000009.11:g.131303352_131303354delinsTTC , CM000671.1:g.131303352_131303354delinsTTC	GRCh37
NC_000009.10:g.130343173_130343175delinsTTC	NCBI36
NG_012073.1:g.41382_41384delinsTTC , LRG_484:g.41382_41384delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1100-29_*1100-27delinsTTC	ENSP00000507095.1:n.*1100-29_*1100-27delinsTTC
ENST00000683288.1:c.*2028-29_*2028-27delinsTTC	ENSP00000507477.1:n.*2028-29_*2028-27delinsTTC
ENST00000683748.1:c.2056-29_2056-27delinsTTC	ENSP00000507377.1:n.2056-29_2056-27delinsTTC
ENST00000683905.1:c.*705-29_*705-27delinsTTC	ENSP00000506960.1:n.*705-29_*705-27delinsTTC
ENST00000684139.1:c.1564-29_1564-27delinsTTC	ENSP00000507295.1:n.1564-29_1564-27delinsTTC
ENST00000684210.1:n.1742-29_1742-27delinsTTC
ENST00000684314.1:c.1924-29_1924-27delinsTTC	ENSP00000507700.1:n.1924-29_1924-27delinsTTC
ENST00000684331.1:c.*720_*722delinsTTC	ENSP00000507431.1:n.*720_*722delinsTTC
ENST00000684463.1:n.667-29_667-27delinsTTC
ENST00000684646.1:c.1816-29_1816-27delinsTTC	ENSP00000507723.1:n.1816-29_1816-27delinsTTC
ENST00000309971.9:c.2029-29_2029-27delinsTTC MANE Select	ENSP00000308622.5:n.2029-29_2029-27delinsTTC
ENST00000309971.8:c.2029-29_2029-27delinsTTC	ENSP00000308622.4:n.2029-29_2029-27delinsTTC
NM_001003722.1:c.2029-29_2029-27delinsTTC , LRG_484t1:c.2029-29_2029-27delinsTTC	NP_001003722.1:n.2029-29_2029-27delinsTTC
XM_006717059.2:c.2065-29_2065-27delinsTTC	XP_006717122.1:n.2065-29_2065-27delinsTTC
XM_006717060.2:c.2038-29_2038-27delinsTTC	XP_006717123.1:n.2038-29_2038-27delinsTTC
XM_011518549.1:c.2065-29_2065-27delinsTTC	XP_011516851.1:n.2065-29_2065-27delinsTTC
XM_011518550.1:c.2065-29_2065-27delinsTTC	XP_011516852.1:n.2065-29_2065-27delinsTTC
XM_011518551.1:c.2056-29_2056-27delinsTTC	XP_011516853.1:n.2056-29_2056-27delinsTTC
XM_011518552.1:c.1306-29_1306-27delinsTTC	XP_011516854.1:n.1306-29_1306-27delinsTTC
XR_242681.3:n.100+2304_100+2306delinsGAA
XR_428600.2:n.19_21delinsGAA
XM_006717059.3:c.2065-29_2065-27delinsTTC	XP_006717122.1:n.2065-29_2065-27delinsTTC
XM_006717060.3:c.2038-29_2038-27delinsTTC	XP_006717123.1:n.2038-29_2038-27delinsTTC
XM_011518551.2:c.2056-29_2056-27delinsTTC	XP_011516853.1:n.2056-29_2056-27delinsTTC
XM_024447519.1:c.2038-29_2038-27delinsTTC	XP_024303287.1:n.2038-29_2038-27delinsTTC
XR_428600.3:n.21_23delinsGAA
NM_001003722.2:c.2029-29_2029-27delinsTTC MANE Select	NP_001003722.1:n.2029-29_2029-27delinsTTC