Canonical Allele Identifier: CA375046295

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131302616A>C (hg19) ; chr9:g.128540337A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540337A>C , CM000671.2:g.128540337A>C	GRCh38
NC_000009.11:g.131302616A>C , CM000671.1:g.131302616A>C	GRCh37
NC_000009.10:g.130342437A>C	NCBI36
NG_012073.1:g.40646A>C , LRG_484:g.40646A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1098A>C	ENSP00000507095.1:n.*1098A>C
ENST00000683288.1:c.*2026A>C	ENSP00000507477.1:n.*2026A>C
ENST00000683748.1:c.2054A>C	ENSP00000507377.1:p.Glu685Ala
ENST00000683905.1:c.*703A>C	ENSP00000506960.1:n.*703A>C
ENST00000684139.1:c.1562A>C	ENSP00000507295.1:p.Glu521Ala
ENST00000684210.1:n.1740A>C
ENST00000684314.1:c.1922A>C	ENSP00000507700.1:p.Glu641Ala
ENST00000684331.1:c.2027A>C	ENSP00000507431.1:p.Glu676Ala
ENST00000684463.1:n.665A>C
ENST00000684646.1:c.1814A>C	ENSP00000507723.1:p.Glu605Ala
ENST00000309971.9:c.2027A>C MANE Select	ENSP00000308622.5:p.Glu676Ala
ENST00000309971.8:c.2027A>C	ENSP00000308622.4:p.Glu676Ala
NM_001003722.1:c.2027A>C , LRG_484t1:c.2027A>C	NP_001003722.1:p.Glu676Ala
XM_006717059.2:c.2063A>C	XP_006717122.1:p.Glu688Ala
XM_006717060.2:c.2036A>C	XP_006717123.1:p.Glu679Ala
XM_011518549.1:c.2063A>C	XP_011516851.1:p.Glu688Ala
XM_011518550.1:c.2063A>C	XP_011516852.1:p.Glu688Ala
XM_011518551.1:c.2054A>C	XP_011516853.1:p.Glu685Ala
XM_011518552.1:c.1304A>C	XP_011516854.1:p.Glu435Ala
XR_242681.3:n.100+3042T>G
XR_428600.2:n.124+633T>G
XM_006717059.3:c.2063A>C	XP_006717122.1:p.Glu688Ala
XM_006717060.3:c.2036A>C	XP_006717123.1:p.Glu679Ala
XM_011518551.2:c.2054A>C	XP_011516853.1:p.Glu685Ala
XM_024447519.1:c.2036A>C	XP_024303287.1:p.Glu679Ala
XR_428600.3:n.126+633T>G
NM_001003722.2:c.2027A>C MANE Select	NP_001003722.1:p.Glu676Ala