Canonical Allele Identifier: CA2201614562

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362067A= , CM000678.2:g.1362067A=	GRCh38
NC_000016.9:g.1412068A= , CM000678.1:g.1412068A=	GRCh37
NC_000016.8:g.1352069A=	NCBI36
NG_016985.1:g.15169A=
NG_033129.1:g.57638T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.446A=
ENST00000529110.2:c.431A=	ENSP00000435349.2:p.Asn144=
ENST00000529957.6:n.405A=
ENST00000683366.1:c.*79A=	ENSP00000507283.1:n.*79A=
ENST00000683887.1:c.395A=	ENSP00000506886.1:p.Asn132=
ENST00000684100.1:n.341A=
ENST00000684126.1:n.405A=
ENST00000684688.1:n.972A=
ENST00000204679.9:c.347A= MANE Select	ENSP00000204679.4:p.Asn116=
ENST00000204679.8:c.347A=	ENSP00000204679.4:p.Asn116=
ENST00000526820.5:c.*249A=	ENSP00000434413.1:n.*249A=
ENST00000527076.1:n.1363A=
ENST00000527168.5:n.383A=
ENST00000529110.1:c.414A=
ENST00000529957.5:n.446A=
NM_032520.4:c.347A=	NP_115909.1:p.Asn116=
XM_017023782.1:c.395A=	XP_016879271.1:p.Asn132=
XM_017023783.1:c.-14A=	XP_016879272.1:n.-14A=
NM_032520.5:c.347A= MANE Select	NP_115909.1:p.Asn116=