Canonical Allele Identifier: CA375046311

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131303382A>C (hg19) ; chr9:g.128541103A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541103A>C , CM000671.2:g.128541103A>C	GRCh38
NC_000009.11:g.131303382A>C , CM000671.1:g.131303382A>C	GRCh37
NC_000009.10:g.130343203A>C	NCBI36
NG_012073.1:g.41412A>C , LRG_484:g.41412A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1101A>C	ENSP00000507095.1:n.*1101A>C
ENST00000683288.1:c.*2029A>C	ENSP00000507477.1:n.*2029A>C
ENST00000683748.1:c.2057A>C	ENSP00000507377.1:p.Lys686Thr
ENST00000683905.1:c.*706A>C	ENSP00000506960.1:n.*706A>C
ENST00000684139.1:c.1565A>C	ENSP00000507295.1:p.Lys522Thr
ENST00000684210.1:n.1743A>C
ENST00000684314.1:c.1925A>C	ENSP00000507700.1:p.Lys642Thr
ENST00000684331.1:c.*750A>C	ENSP00000507431.1:n.*750A>C
ENST00000684463.1:n.668A>C
ENST00000684646.1:c.1817A>C	ENSP00000507723.1:p.Lys606Thr
ENST00000309971.9:c.2030A>C MANE Select	ENSP00000308622.5:p.Lys677Thr
ENST00000309971.8:c.2030A>C	ENSP00000308622.4:p.Lys677Thr
NM_001003722.1:c.2030A>C , LRG_484t1:c.2030A>C	NP_001003722.1:p.Lys677Thr
XM_006717059.2:c.2066A>C	XP_006717122.1:p.Lys689Thr
XM_006717060.2:c.2039A>C	XP_006717123.1:p.Lys680Thr
XM_011518549.1:c.2066A>C	XP_011516851.1:p.Lys689Thr
XM_011518550.1:c.2066A>C	XP_011516852.1:p.Lys689Thr
XM_011518551.1:c.2057A>C	XP_011516853.1:p.Lys686Thr
XM_011518552.1:c.1307A>C	XP_011516854.1:p.Lys436Thr
XR_242681.3:n.100+2276T>G
XM_006717059.3:c.2066A>C	XP_006717122.1:p.Lys689Thr
XM_006717060.3:c.2039A>C	XP_006717123.1:p.Lys680Thr
XM_011518551.2:c.2057A>C	XP_011516853.1:p.Lys686Thr
XM_024447519.1:c.2039A>C	XP_024303287.1:p.Lys680Thr
NM_001003722.2:c.2030A>C MANE Select	NP_001003722.1:p.Lys677Thr