Canonical Allele Identifier: CA375046309
Gene: GLE1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128541102A>G , CM000671.2:g.128541102A>G GRCh38
NC_000009.11:g.131303381A>G , CM000671.1:g.131303381A>G GRCh37
NC_000009.10:g.130343202A>G NCBI36
NG_012073.1:g.41411A>G , LRG_484:g.41411A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000683044.1:c.*1100A>G ENSP00000507095.1:n.*1100A>G
ENST00000683288.1:c.*2028A>G ENSP00000507477.1:n.*2028A>G
ENST00000683748.1:c.2056A>G ENSP00000507377.1:p.Lys686Glu
ENST00000683905.1:c.*705A>G ENSP00000506960.1:n.*705A>G
ENST00000684139.1:c.1564A>G ENSP00000507295.1:p.Lys522Glu
ENST00000684210.1:n.1742A>G
ENST00000684314.1:c.1924A>G ENSP00000507700.1:p.Lys642Glu
ENST00000684331.1:c.*749A>G ENSP00000507431.1:n.*749A>G
ENST00000684463.1:n.667A>G
ENST00000684646.1:c.1816A>G ENSP00000507723.1:p.Lys606Glu
ENST00000309971.9:c.2029A>G MANE Select ENSP00000308622.5:p.Lys677Glu
ENST00000309971.8:c.2029A>G ENSP00000308622.4:p.Lys677Glu
NM_001003722.1:c.2029A>G , LRG_484t1:c.2029A>G NP_001003722.1:p.Lys677Glu
XM_006717059.2:c.2065A>G XP_006717122.1:p.Lys689Glu
XM_006717060.2:c.2038A>G XP_006717123.1:p.Lys680Glu
XM_011518549.1:c.2065A>G XP_011516851.1:p.Lys689Glu
XM_011518550.1:c.2065A>G XP_011516852.1:p.Lys689Glu
XM_011518551.1:c.2056A>G XP_011516853.1:p.Lys686Glu
XM_011518552.1:c.1306A>G XP_011516854.1:p.Lys436Glu
XR_242681.3:n.100+2277T>C
XM_006717059.3:c.2065A>G XP_006717122.1:p.Lys689Glu
XM_006717060.3:c.2038A>G XP_006717123.1:p.Lys680Glu
XM_011518551.2:c.2056A>G XP_011516853.1:p.Lys686Glu
XM_024447519.1:c.2038A>G XP_024303287.1:p.Lys680Glu
NM_001003722.2:c.2029A>G MANE Select NP_001003722.1:p.Lys677Glu