Canonical Allele Identifier: CA467287278

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131302943A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540664A>T , CM000671.2:g.128540664A>T	GRCh38
NC_000009.11:g.131302943A>T , CM000671.1:g.131302943A>T	GRCh37
NC_000009.10:g.130342764A>T	NCBI36
NG_012073.1:g.40973A>T , LRG_484:g.40973A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1099+326A>T	ENSP00000507095.1:n.*1099+326A>T
ENST00000683288.1:c.*2027+326A>T	ENSP00000507477.1:n.*2027+326A>T
ENST00000683748.1:c.2055+326A>T	ENSP00000507377.1:n.2055+326A>T
ENST00000683905.1:c.*704+326A>T	ENSP00000506960.1:n.*704+326A>T
ENST00000684139.1:c.1563+326A>T	ENSP00000507295.1:n.1563+326A>T
ENST00000684210.1:n.1741+326A>T
ENST00000684314.1:c.1923+326A>T	ENSP00000507700.1:n.1923+326A>T
ENST00000684331.1:c.*311A>T	ENSP00000507431.1:n.*311A>T
ENST00000684463.1:n.666+326A>T
ENST00000684646.1:c.1815+326A>T	ENSP00000507723.1:n.1815+326A>T
ENST00000309971.9:c.2028+326A>T MANE Select	ENSP00000308622.5:n.2028+326A>T
ENST00000309971.8:c.2028+326A>T	ENSP00000308622.4:n.2028+326A>T
NM_001003722.1:c.2028+326A>T , LRG_484t1:c.2028+326A>T	NP_001003722.1:n.2028+326A>T
XM_006717059.2:c.2064+326A>T	XP_006717122.1:n.2064+326A>T
XM_006717060.2:c.2037+326A>T	XP_006717123.1:n.2037+326A>T
XM_011518549.1:c.2064+326A>T	XP_011516851.1:n.2064+326A>T
XM_011518550.1:c.2064+326A>T	XP_011516852.1:n.2064+326A>T
XM_011518551.1:c.2055+326A>T	XP_011516853.1:n.2055+326A>T
XM_011518552.1:c.1305+326A>T	XP_011516854.1:n.1305+326A>T
XR_242681.3:n.100+2715T>A
XR_428600.2:n.124+306T>A
XM_006717059.3:c.2064+326A>T	XP_006717122.1:n.2064+326A>T
XM_006717060.3:c.2037+326A>T	XP_006717123.1:n.2037+326A>T
XM_011518551.2:c.2055+326A>T	XP_011516853.1:n.2055+326A>T
XM_024447519.1:c.2037+326A>T	XP_024303287.1:n.2037+326A>T
XR_428600.3:n.126+306T>A
NM_001003722.2:c.2028+326A>T MANE Select	NP_001003722.1:n.2028+326A>T