Canonical Allele Identifier: CA375046342

Gene: GLE1

Linked Data

• MyVariant Identifiers: chr9:g.131303394A>C (hg19) ; chr9:g.128541115A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541115A>C , CM000671.2:g.128541115A>C	GRCh38
NC_000009.11:g.131303394A>C , CM000671.1:g.131303394A>C	GRCh37
NC_000009.10:g.130343215A>C	NCBI36
NG_012073.1:g.41424A>C , LRG_484:g.41424A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1113A>C	ENSP00000507095.1:n.*1113A>C
ENST00000683288.1:c.*2041A>C	ENSP00000507477.1:n.*2041A>C
ENST00000683748.1:c.2069A>C	ENSP00000507377.1:p.His690Pro
ENST00000683905.1:c.*718A>C	ENSP00000506960.1:n.*718A>C
ENST00000684139.1:c.1577A>C	ENSP00000507295.1:p.His526Pro
ENST00000684210.1:n.1755A>C
ENST00000684314.1:c.1937A>C	ENSP00000507700.1:p.His646Pro
ENST00000684331.1:c.*762A>C	ENSP00000507431.1:n.*762A>C
ENST00000684463.1:n.680A>C
ENST00000684646.1:c.1829A>C	ENSP00000507723.1:p.His610Pro
ENST00000309971.9:c.2042A>C MANE Select	ENSP00000308622.5:p.His681Pro
ENST00000309971.8:c.2042A>C	ENSP00000308622.4:p.His681Pro
NM_001003722.1:c.2042A>C , LRG_484t1:c.2042A>C	NP_001003722.1:p.His681Pro
XM_006717059.2:c.2078A>C	XP_006717122.1:p.His693Pro
XM_006717060.2:c.2051A>C	XP_006717123.1:p.His684Pro
XM_011518549.1:c.2078A>C	XP_011516851.1:p.His693Pro
XM_011518550.1:c.2078A>C	XP_011516852.1:p.His693Pro
XM_011518551.1:c.2069A>C	XP_011516853.1:p.His690Pro
XM_011518552.1:c.1319A>C	XP_011516854.1:p.His440Pro
XR_242681.3:n.100+2264T>G
XM_006717059.3:c.2078A>C	XP_006717122.1:p.His693Pro
XM_006717060.3:c.2051A>C	XP_006717123.1:p.His684Pro
XM_011518551.2:c.2069A>C	XP_011516853.1:p.His690Pro
XM_024447519.1:c.2051A>C	XP_024303287.1:p.His684Pro
NM_001003722.2:c.2042A>C MANE Select	NP_001003722.1:p.His681Pro