Canonical Allele Identifier: CA467288253

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131303195G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540916G>A , CM000671.2:g.128540916G>A	GRCh38
NC_000009.11:g.131303195G>A , CM000671.1:g.131303195G>A	GRCh37
NC_000009.10:g.130343016G>A	NCBI36
NG_012073.1:g.41225G>A , LRG_484:g.41225G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1100-186G>A	ENSP00000507095.1:n.*1100-186G>A
ENST00000683288.1:c.*2028-186G>A	ENSP00000507477.1:n.*2028-186G>A
ENST00000683748.1:c.2056-186G>A	ENSP00000507377.1:n.2056-186G>A
ENST00000683905.1:c.*705-186G>A	ENSP00000506960.1:n.*705-186G>A
ENST00000684139.1:c.1564-186G>A	ENSP00000507295.1:n.1564-186G>A
ENST00000684210.1:n.1742-186G>A
ENST00000684314.1:c.1924-186G>A	ENSP00000507700.1:n.1924-186G>A
ENST00000684331.1:c.*563G>A	ENSP00000507431.1:n.*563G>A
ENST00000684463.1:n.667-186G>A
ENST00000684646.1:c.1816-186G>A	ENSP00000507723.1:n.1816-186G>A
ENST00000309971.9:c.2029-186G>A MANE Select	ENSP00000308622.5:n.2029-186G>A
ENST00000309971.8:c.2029-186G>A	ENSP00000308622.4:n.2029-186G>A
NM_001003722.1:c.2029-186G>A , LRG_484t1:c.2029-186G>A	NP_001003722.1:n.2029-186G>A
XM_006717059.2:c.2065-186G>A	XP_006717122.1:n.2065-186G>A
XM_006717060.2:c.2038-186G>A	XP_006717123.1:n.2038-186G>A
XM_011518549.1:c.2065-186G>A	XP_011516851.1:n.2065-186G>A
XM_011518550.1:c.2065-186G>A	XP_011516852.1:n.2065-186G>A
XM_011518551.1:c.2056-186G>A	XP_011516853.1:n.2056-186G>A
XM_011518552.1:c.1306-186G>A	XP_011516854.1:n.1306-186G>A
XR_242681.3:n.100+2463C>T
XR_428600.2:n.124+54C>T
XM_006717059.3:c.2065-186G>A	XP_006717122.1:n.2065-186G>A
XM_006717060.3:c.2038-186G>A	XP_006717123.1:n.2038-186G>A
XM_011518551.2:c.2056-186G>A	XP_011516853.1:n.2056-186G>A
XM_024447519.1:c.2038-186G>A	XP_024303287.1:n.2038-186G>A
XR_428600.3:n.126+54C>T
NM_001003722.2:c.2029-186G>A MANE Select	NP_001003722.1:n.2029-186G>A