Canonical Allele Identifier: CA2201614133
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1361907C= , CM000678.2:g.1361907C= GRCh38
NC_000016.9:g.1411908C= , CM000678.1:g.1411908C= GRCh37
NC_000016.8:g.1351909C= NCBI36
NG_016985.1:g.15009C=
NG_033129.1:g.57798G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.368C=
ENST00000529110.2:c.353C= ENSP00000435349.2:p.Thr118=
ENST00000529957.6:n.327C=
ENST00000683366.1:c.*1C= ENSP00000507283.1:n.*1C=
ENST00000683887.1:c.317C= ENSP00000506886.1:p.Thr106=
ENST00000684100.1:n.263C=
ENST00000684126.1:n.327C=
ENST00000684688.1:n.894C=
ENST00000204679.9:c.269C= MANE Select ENSP00000204679.4:p.Thr90=
ENST00000204679.8:c.269C= ENSP00000204679.4:p.Thr90=
ENST00000526820.5:c.*171C= ENSP00000434413.1:n.*171C=
ENST00000527076.1:n.1285C=
ENST00000527168.5:n.305C=
ENST00000529110.1:c.336C=
ENST00000529957.5:n.368C=
NM_032520.4:c.269C= NP_115909.1:p.Thr90=
XM_017023782.1:c.317C= XP_016879271.1:p.Thr106=
XM_017023783.1:c.-92C= XP_016879272.1:n.-92C=
NM_032520.5:c.269C= MANE Select NP_115909.1:p.Thr90=