Canonical Allele Identifier: CA375046237

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131302591T>C (hg19) ; chr9:g.128540312T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128540312T>C , CM000671.2:g.128540312T>C	GRCh38
NC_000009.11:g.131302591T>C , CM000671.1:g.131302591T>C	GRCh37
NC_000009.10:g.130342412T>C	NCBI36
NG_012073.1:g.40621T>C , LRG_484:g.40621T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1073T>C	ENSP00000507095.1:n.*1073T>C
ENST00000683288.1:c.*2001T>C	ENSP00000507477.1:n.*2001T>C
ENST00000683748.1:c.2029T>C	ENSP00000507377.1:p.Phe677Leu
ENST00000683905.1:c.*678T>C	ENSP00000506960.1:n.*678T>C
ENST00000684139.1:c.1537T>C	ENSP00000507295.1:p.Phe513Leu
ENST00000684210.1:n.1715T>C
ENST00000684314.1:c.1897T>C	ENSP00000507700.1:p.Phe633Leu
ENST00000684331.1:c.2002T>C	ENSP00000507431.1:p.Phe668Leu
ENST00000684463.1:n.640T>C
ENST00000684646.1:c.1789T>C	ENSP00000507723.1:p.Phe597Leu
ENST00000309971.9:c.2002T>C MANE Select	ENSP00000308622.5:p.Phe668Leu
ENST00000309971.8:c.2002T>C	ENSP00000308622.4:p.Phe668Leu
NM_001003722.1:c.2002T>C , LRG_484t1:c.2002T>C	NP_001003722.1:p.Phe668Leu
XM_006717059.2:c.2038T>C	XP_006717122.1:p.Phe680Leu
XM_006717060.2:c.2011T>C	XP_006717123.1:p.Phe671Leu
XM_011518549.1:c.2038T>C	XP_011516851.1:p.Phe680Leu
XM_011518550.1:c.2038T>C	XP_011516852.1:p.Phe680Leu
XM_011518551.1:c.2029T>C	XP_011516853.1:p.Phe677Leu
XM_011518552.1:c.1279T>C	XP_011516854.1:p.Phe427Leu
XR_242681.3:n.100+3067A>G
XR_428600.2:n.124+658A>G
XM_006717059.3:c.2038T>C	XP_006717122.1:p.Phe680Leu
XM_006717060.3:c.2011T>C	XP_006717123.1:p.Phe671Leu
XM_011518551.2:c.2029T>C	XP_011516853.1:p.Phe677Leu
XM_024447519.1:c.2011T>C	XP_024303287.1:p.Phe671Leu
XR_428600.3:n.126+658A>G
NM_001003722.2:c.2002T>C MANE Select	NP_001003722.1:p.Phe668Leu