Canonical Allele Identifier: CA2201615335

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362715G= , CM000678.2:g.1362715G=	GRCh38
NC_000016.9:g.1412716G= , CM000678.1:g.1412716G=	GRCh37
NC_000016.8:g.1352717G=	NCBI36
NG_016985.1:g.15817G=
NG_033129.1:g.56990C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.813G=
ENST00000529110.2:c.798G=	ENSP00000435349.2:p.Gly266=
ENST00000529957.6:n.772G=
ENST00000683366.1:c.*446G=	ENSP00000507283.1:n.*446G=
ENST00000683887.1:c.762G=	ENSP00000506886.1:p.Gly254=
ENST00000684100.1:n.708G=
ENST00000684126.1:n.848G=
ENST00000684688.1:n.1339G=
ENST00000204679.9:c.714G= MANE Select	ENSP00000204679.4:p.Gly238=
ENST00000204679.8:c.714G=	ENSP00000204679.4:p.Gly238=
ENST00000527076.1:n.1937G=
ENST00000527168.5:n.881G=
ENST00000529957.5:n.813G=
NM_032520.4:c.714G=	NP_115909.1:p.Gly238=
XM_017023782.1:c.762G=	XP_016879271.1:p.Gly254=
XM_017023783.1:c.354G=	XP_016879272.1:p.Gly118=
NM_032520.5:c.714G= MANE Select	NP_115909.1:p.Gly238=