Canonical Allele Identifier: CA2201615191
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362525C= , CM000678.2:g.1362525C= GRCh38
NC_000016.9:g.1412526C= , CM000678.1:g.1412526C= GRCh37
NC_000016.8:g.1352527C= NCBI36
NG_016985.1:g.15627C=
NG_033129.1:g.57180G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.699C=
ENST00000529110.2:c.684C= ENSP00000435349.2:p.Ile228=
ENST00000529957.6:n.658C=
ENST00000683366.1:c.*332C= ENSP00000507283.1:n.*332C=
ENST00000683887.1:c.648C= ENSP00000506886.1:p.Ile216=
ENST00000684100.1:n.594C=
ENST00000684126.1:n.658C=
ENST00000684688.1:n.1225C=
ENST00000204679.9:c.600C= MANE Select ENSP00000204679.4:p.Ile200=
ENST00000204679.8:c.600C= ENSP00000204679.4:p.Ile200=
ENST00000527076.1:n.1747C=
ENST00000527168.5:n.767C=
ENST00000529957.5:n.699C=
NM_032520.4:c.600C= NP_115909.1:p.Ile200=
XM_017023782.1:c.648C= XP_016879271.1:p.Ile216=
XM_017023783.1:c.240C= XP_016879272.1:p.Ile80=
NM_032520.5:c.600C= MANE Select NP_115909.1:p.Ile200=