Canonical Allele Identifier: CA1880333237

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541079_128541082delinsTTTC , CM000671.2:g.128541079_128541082delinsTTTC	GRCh38
NC_000009.11:g.131303358_131303361delinsTTTC , CM000671.1:g.131303358_131303361delinsTTTC	GRCh37
NC_000009.10:g.130343179_130343182delinsTTTC	NCBI36
NG_012073.1:g.41388_41391delinsTTTC , LRG_484:g.41388_41391delinsTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1100-23_*1100-20delinsTTTC	ENSP00000507095.1:n.*1100-23_*1100-20delinsTTTC
ENST00000683288.1:c.*2028-23_*2028-20delinsTTTC	ENSP00000507477.1:n.*2028-23_*2028-20delinsTTTC
ENST00000683748.1:c.2056-23_2056-20delinsTTTC	ENSP00000507377.1:n.2056-23_2056-20delinsTTTC
ENST00000683905.1:c.*705-23_*705-20delinsTTTC	ENSP00000506960.1:n.*705-23_*705-20delinsTTTC
ENST00000684139.1:c.1564-23_1564-20delinsTTTC	ENSP00000507295.1:n.1564-23_1564-20delinsTTTC
ENST00000684210.1:n.1742-23_1742-20delinsTTTC
ENST00000684314.1:c.1924-23_1924-20delinsTTTC	ENSP00000507700.1:n.1924-23_1924-20delinsTTTC
ENST00000684331.1:c.*726_*729delinsTTTC	ENSP00000507431.1:n.*726_*729delinsTTTC
ENST00000684463.1:n.667-23_667-20delinsTTTC
ENST00000684646.1:c.1816-23_1816-20delinsTTTC	ENSP00000507723.1:n.1816-23_1816-20delinsTTTC
ENST00000309971.9:c.2029-23_2029-20delinsTTTC MANE Select	ENSP00000308622.5:n.2029-23_2029-20delinsTTTC
ENST00000309971.8:c.2029-23_2029-20delinsTTTC	ENSP00000308622.4:n.2029-23_2029-20delinsTTTC
NM_001003722.1:c.2029-23_2029-20delinsTTTC , LRG_484t1:c.2029-23_2029-20delinsTTTC	NP_001003722.1:n.2029-23_2029-20delinsTTTC
XM_006717059.2:c.2065-23_2065-20delinsTTTC	XP_006717122.1:n.2065-23_2065-20delinsTTTC
XM_006717060.2:c.2038-23_2038-20delinsTTTC	XP_006717123.1:n.2038-23_2038-20delinsTTTC
XM_011518549.1:c.2065-23_2065-20delinsTTTC	XP_011516851.1:n.2065-23_2065-20delinsTTTC
XM_011518550.1:c.2065-23_2065-20delinsTTTC	XP_011516852.1:n.2065-23_2065-20delinsTTTC
XM_011518551.1:c.2056-23_2056-20delinsTTTC	XP_011516853.1:n.2056-23_2056-20delinsTTTC
XM_011518552.1:c.1306-23_1306-20delinsTTTC	XP_011516854.1:n.1306-23_1306-20delinsTTTC
XR_242681.3:n.100+2297_100+2300delinsGAAA
XR_428600.2:n.12_15delinsGAAA
XM_006717059.3:c.2065-23_2065-20delinsTTTC	XP_006717122.1:n.2065-23_2065-20delinsTTTC
XM_006717060.3:c.2038-23_2038-20delinsTTTC	XP_006717123.1:n.2038-23_2038-20delinsTTTC
XM_011518551.2:c.2056-23_2056-20delinsTTTC	XP_011516853.1:n.2056-23_2056-20delinsTTTC
XM_024447519.1:c.2038-23_2038-20delinsTTTC	XP_024303287.1:n.2038-23_2038-20delinsTTTC
XR_428600.3:n.14_17delinsGAAA
NM_001003722.2:c.2029-23_2029-20delinsTTTC MANE Select	NP_001003722.1:n.2029-23_2029-20delinsTTTC