Canonical Allele Identifier: CA2201615284
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362641G= , CM000678.2:g.1362641G= GRCh38
NC_000016.9:g.1412642G= , CM000678.1:g.1412642G= GRCh37
NC_000016.8:g.1352643G= NCBI36
NG_016985.1:g.15743G=
NG_033129.1:g.57064C=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.739G=
ENST00000529110.2:c.724G= ENSP00000435349.2:p.Glu242=
ENST00000529957.6:n.698G=
ENST00000683366.1:c.*372G= ENSP00000507283.1:n.*372G=
ENST00000683887.1:c.688G= ENSP00000506886.1:p.Glu230=
ENST00000684100.1:n.634G=
ENST00000684126.1:n.774G=
ENST00000684688.1:n.1265G=
ENST00000204679.9:c.640G= MANE Select ENSP00000204679.4:p.Glu214=
ENST00000204679.8:c.640G= ENSP00000204679.4:p.Glu214=
ENST00000527076.1:n.1863G=
ENST00000527168.5:n.807G=
ENST00000529957.5:n.739G=
NM_032520.4:c.640G= NP_115909.1:p.Glu214=
XM_017023782.1:c.688G= XP_016879271.1:p.Glu230=
XM_017023783.1:c.280G= XP_016879272.1:p.Glu94=
NM_032520.5:c.640G= MANE Select NP_115909.1:p.Glu214=