Canonical Allele Identifier: CA1880332792

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540661_128540665delinsGGTAA , CM000671.2:g.128540661_128540665delinsGGTAA	GRCh38
NC_000009.11:g.131302940_131302944delinsGGTAA , CM000671.1:g.131302940_131302944delinsGGTAA	GRCh37
NC_000009.10:g.130342761_130342765delinsGGTAA	NCBI36
NG_012073.1:g.40970_40974delinsGGTAA , LRG_484:g.40970_40974delinsGGTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1099+323_*1099+327delinsGGTAA	ENSP00000507095.1:n.*1099+323_*1099+327delinsGGTAA
ENST00000683288.1:c.*2027+323_*2027+327delinsGGTAA	ENSP00000507477.1:n.*2027+323_*2027+327delinsGGTAA
ENST00000683748.1:c.2055+323_2055+327delinsGGTAA	ENSP00000507377.1:n.2055+323_2055+327delinsGGTAA
ENST00000683905.1:c.*704+323_*704+327delinsGGTAA	ENSP00000506960.1:n.*704+323_*704+327delinsGGTAA
ENST00000684139.1:c.1563+323_1563+327delinsGGTAA	ENSP00000507295.1:n.1563+323_1563+327delinsGGTAA
ENST00000684210.1:n.1741+323_1741+327delinsGGTAA
ENST00000684314.1:c.1923+323_1923+327delinsGGTAA	ENSP00000507700.1:n.1923+323_1923+327delinsGGTAA
ENST00000684331.1:c.*308_*312delinsGGTAA	ENSP00000507431.1:n.*308_*312delinsGGTAA
ENST00000684463.1:n.666+323_666+327delinsGGTAA
ENST00000684646.1:c.1815+323_1815+327delinsGGTAA	ENSP00000507723.1:n.1815+323_1815+327delinsGGTAA
ENST00000309971.9:c.2028+323_2028+327delinsGGTAA MANE Select	ENSP00000308622.5:n.2028+323_2028+327delinsGGTAA
ENST00000309971.8:c.2028+323_2028+327delinsGGTAA	ENSP00000308622.4:n.2028+323_2028+327delinsGGTAA
NM_001003722.1:c.2028+323_2028+327delinsGGTAA , LRG_484t1:c.2028+323_2028+327delinsGGTAA	NP_001003722.1:n.2028+323_2028+327delinsGGTAA
XM_006717059.2:c.2064+323_2064+327delinsGGTAA	XP_006717122.1:n.2064+323_2064+327delinsGGTAA
XM_006717060.2:c.2037+323_2037+327delinsGGTAA	XP_006717123.1:n.2037+323_2037+327delinsGGTAA
XM_011518549.1:c.2064+323_2064+327delinsGGTAA	XP_011516851.1:n.2064+323_2064+327delinsGGTAA
XM_011518550.1:c.2064+323_2064+327delinsGGTAA	XP_011516852.1:n.2064+323_2064+327delinsGGTAA
XM_011518551.1:c.2055+323_2055+327delinsGGTAA	XP_011516853.1:n.2055+323_2055+327delinsGGTAA
XM_011518552.1:c.1305+323_1305+327delinsGGTAA	XP_011516854.1:n.1305+323_1305+327delinsGGTAA
XR_242681.3:n.100+2714_100+2718delinsTTACC
XR_428600.2:n.124+305_124+309delinsTTACC
XM_006717059.3:c.2064+323_2064+327delinsGGTAA	XP_006717122.1:n.2064+323_2064+327delinsGGTAA
XM_006717060.3:c.2037+323_2037+327delinsGGTAA	XP_006717123.1:n.2037+323_2037+327delinsGGTAA
XM_011518551.2:c.2055+323_2055+327delinsGGTAA	XP_011516853.1:n.2055+323_2055+327delinsGGTAA
XM_024447519.1:c.2037+323_2037+327delinsGGTAA	XP_024303287.1:n.2037+323_2037+327delinsGGTAA
XR_428600.3:n.126+305_126+309delinsTTACC
NM_001003722.2:c.2028+323_2028+327delinsGGTAA MANE Select	NP_001003722.1:n.2028+323_2028+327delinsGGTAA