Canonical Allele Identifier: CA1880333309

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541139_128541143delinsGCTTT , CM000671.2:g.128541139_128541143delinsGCTTT	GRCh38
NC_000009.11:g.131303418_131303422delinsGCTTT , CM000671.1:g.131303418_131303422delinsGCTTT	GRCh37
NC_000009.10:g.130343239_130343243delinsGCTTT	NCBI36
NG_012073.1:g.41448_41452delinsGCTTT , LRG_484:g.41448_41452delinsGCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1137_*1141delinsGCTTT	ENSP00000507095.1:n.*1137_*1141delinsGCTTT
ENST00000683288.1:c.*2065_*2069delinsGCTTT	ENSP00000507477.1:n.*2065_*2069delinsGCTTT
ENST00000683748.1:c.2093_2097delinsGCTTT	ENSP00000507377.1:p.Gly698=
ENST00000683905.1:c.*742_*746delinsGCTTT	ENSP00000506960.1:n.*742_*746delinsGCTTT
ENST00000684139.1:c.1601_1605delinsGCTTT	ENSP00000507295.1:p.Gly534=
ENST00000684210.1:n.1779_1783delinsGCTTT
ENST00000684314.1:c.1961_1965delinsGCTTT	ENSP00000507700.1:p.Gly654=
ENST00000684331.1:c.*786_*790delinsGCTTT	ENSP00000507431.1:n.*786_*790delinsGCTTT
ENST00000684463.1:n.704_708delinsGCTTT
ENST00000684646.1:c.1853_1857delinsGCTTT	ENSP00000507723.1:p.Gly618=
ENST00000309971.9:c.2066_2070delinsGCTTT MANE Select	ENSP00000308622.5:p.Gly689=
ENST00000309971.8:c.2066_2070delinsGCTTT	ENSP00000308622.4:p.Gly689=
NM_001003722.1:c.2066_2070delinsGCTTT , LRG_484t1:c.2066_2070delinsGCTTT	NP_001003722.1:p.Gly689=
XM_006717059.2:c.2102_2106delinsGCTTT	XP_006717122.1:p.Gly701=
XM_006717060.2:c.2075_2079delinsGCTTT	XP_006717123.1:p.Gly692=
XM_011518549.1:c.2102_2106delinsGCTTT	XP_011516851.1:p.Gly701=
XM_011518550.1:c.2102_2106delinsGCTTT	XP_011516852.1:p.Gly701=
XM_011518551.1:c.2093_2097delinsGCTTT	XP_011516853.1:p.Gly698=
XM_011518552.1:c.1343_1347delinsGCTTT	XP_011516854.1:p.Gly448=
XR_242681.3:n.100+2236_100+2240delinsAAAGC
XM_006717059.3:c.2102_2106delinsGCTTT	XP_006717122.1:p.Gly701=
XM_006717060.3:c.2075_2079delinsGCTTT	XP_006717123.1:p.Gly692=
XM_011518551.2:c.2093_2097delinsGCTTT	XP_011516853.1:p.Gly698=
XM_024447519.1:c.2075_2079delinsGCTTT	XP_024303287.1:p.Gly692=
NM_001003722.2:c.2066_2070delinsGCTTT MANE Select	NP_001003722.1:p.Gly689=