Canonical Allele Identifier: CA1880333325

Gene: GLE1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128541151C= , CM000671.2:g.128541151C=	GRCh38
NC_000009.11:g.131303430C= , CM000671.1:g.131303430C=	GRCh37
NC_000009.10:g.130343251C=	NCBI36
NG_012073.1:g.41460C= , LRG_484:g.41460C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683044.1:c.*1149C=	ENSP00000507095.1:n.*1149C=
ENST00000683288.1:c.*2077C=	ENSP00000507477.1:n.*2077C=
ENST00000683748.1:c.2105C=	ENSP00000507377.1:p.Ser702=
ENST00000683905.1:c.*754C=	ENSP00000506960.1:n.*754C=
ENST00000684139.1:c.1613C=	ENSP00000507295.1:p.Ser538=
ENST00000684210.1:n.1791C=
ENST00000684314.1:c.1973C=	ENSP00000507700.1:p.Ser658=
ENST00000684331.1:c.*798C=	ENSP00000507431.1:n.*798C=
ENST00000684463.1:n.716C=
ENST00000684646.1:c.1865C=	ENSP00000507723.1:p.Ser622=
ENST00000309971.9:c.2078C= MANE Select	ENSP00000308622.5:p.Ser693=
ENST00000309971.8:c.2078C=	ENSP00000308622.4:p.Ser693=
NM_001003722.1:c.2078C= , LRG_484t1:c.2078C=	NP_001003722.1:p.Ser693=
XM_006717059.2:c.2114C=	XP_006717122.1:p.Ser705=
XM_006717060.2:c.2087C=	XP_006717123.1:p.Ser696=
XM_011518549.1:c.2114C=	XP_011516851.1:p.Ser705=
XM_011518550.1:c.2114C=	XP_011516852.1:p.Ser705=
XM_011518551.1:c.2105C=	XP_011516853.1:p.Ser702=
XM_011518552.1:c.1355C=	XP_011516854.1:p.Ser452=
XR_242681.3:n.100+2228G=
XM_006717059.3:c.2114C=	XP_006717122.1:p.Ser705=
XM_006717060.3:c.2087C=	XP_006717123.1:p.Ser696=
XM_011518551.2:c.2105C=	XP_011516853.1:p.Ser702=
XM_024447519.1:c.2087C=	XP_024303287.1:p.Ser696=
NM_001003722.2:c.2078C= MANE Select	NP_001003722.1:p.Ser693=