Canonical Allele Identifier: CA200395175
Gene: GLE1 HGNC NCBI

Linked Data

dbSNP Id: rs894150130

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128540720dup , CM000671.2:g.128540720dup GRCh38
NC_000009.11:g.131302999dup , CM000671.1:g.131302999dup GRCh37
NC_000009.10:g.130342820dup NCBI36
NG_012073.1:g.41029dup , LRG_484:g.41029dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000683044.1:c.*1100-382dup ENSP00000507095.1:n.*1100-382dup
ENST00000683288.1:c.*2028-382dup ENSP00000507477.1:n.*2028-382dup
ENST00000683748.1:c.2056-382dup ENSP00000507377.1:n.2056-382dup
ENST00000683905.1:c.*705-382dup ENSP00000506960.1:n.*705-382dup
ENST00000684139.1:c.1564-382dup ENSP00000507295.1:n.1564-382dup
ENST00000684210.1:n.1742-382dup
ENST00000684314.1:c.1924-382dup ENSP00000507700.1:n.1924-382dup
ENST00000684331.1:c.*367dup ENSP00000507431.1:n.*367dup
ENST00000684463.1:n.667-382dup
ENST00000684646.1:c.1816-382dup ENSP00000507723.1:n.1816-382dup
ENST00000309971.9:c.2029-382dup MANE Select ENSP00000308622.5:n.2029-382dup
ENST00000309971.8:c.2029-382dup ENSP00000308622.4:n.2029-382dup
NM_001003722.1:c.2029-382dup , LRG_484t1:c.2029-382dup NP_001003722.1:n.2029-382dup
XM_006717059.2:c.2065-382dup XP_006717122.1:n.2065-382dup
XM_006717060.2:c.2038-382dup XP_006717123.1:n.2038-382dup
XM_011518549.1:c.2065-382dup XP_011516851.1:n.2065-382dup
XM_011518550.1:c.2065-382dup XP_011516852.1:n.2065-382dup
XM_011518551.1:c.2056-382dup XP_011516853.1:n.2056-382dup
XM_011518552.1:c.1306-382dup XP_011516854.1:n.1306-382dup
XR_242681.3:n.100+2662dup
XR_428600.2:n.124+253dup
XM_006717059.3:c.2065-382dup XP_006717122.1:n.2065-382dup
XM_006717060.3:c.2038-382dup XP_006717123.1:n.2038-382dup
XM_011518551.2:c.2056-382dup XP_011516853.1:n.2056-382dup
XM_024447519.1:c.2038-382dup XP_024303287.1:n.2038-382dup
XR_428600.3:n.126+253dup
NM_001003722.2:c.2029-382dup MANE Select NP_001003722.1:n.2029-382dup