Canonical Allele Identifier: CA2201614889

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362221G= , CM000678.2:g.1362221G=	GRCh38
NC_000016.9:g.1412222G= , CM000678.1:g.1412222G=	GRCh37
NC_000016.8:g.1352223G=	NCBI36
NG_016985.1:g.15323G=
NG_033129.1:g.57484C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.526G=
ENST00000529110.2:c.511G=	ENSP00000435349.2:p.Gly171=
ENST00000529957.6:n.485G=
ENST00000683366.1:c.*159G=	ENSP00000507283.1:n.*159G=
ENST00000683887.1:c.475G=	ENSP00000506886.1:p.Gly159=
ENST00000684100.1:n.421G=
ENST00000684126.1:n.485G=
ENST00000684688.1:n.1052G=
ENST00000204679.9:c.427G= MANE Select	ENSP00000204679.4:p.Gly143=
ENST00000204679.8:c.427G=	ENSP00000204679.4:p.Gly143=
ENST00000527076.1:n.1443G=
ENST00000527168.5:n.463G=
ENST00000529110.1:c.494G=
ENST00000529957.5:n.526G=
NM_032520.4:c.427G=	NP_115909.1:p.Gly143=
XM_017023782.1:c.475G=	XP_016879271.1:p.Gly159=
XM_017023783.1:c.67G=	XP_016879272.1:p.Gly23=
NM_032520.5:c.427G= MANE Select	NP_115909.1:p.Gly143=