Canonical Allele Identifier: CA2201614138
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1361908C= , CM000678.2:g.1361908C= GRCh38
NC_000016.9:g.1411909C= , CM000678.1:g.1411909C= GRCh37
NC_000016.8:g.1351910C= NCBI36
NG_016985.1:g.15010C=
NG_033129.1:g.57797G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000527168.6:n.369C=
ENST00000529110.2:c.354C= ENSP00000435349.2:p.Thr118=
ENST00000529957.6:n.328C=
ENST00000683366.1:c.*2C= ENSP00000507283.1:n.*2C=
ENST00000683887.1:c.318C= ENSP00000506886.1:p.Thr106=
ENST00000684100.1:n.264C=
ENST00000684126.1:n.328C=
ENST00000684688.1:n.895C=
ENST00000204679.9:c.270C= MANE Select ENSP00000204679.4:p.Thr90=
ENST00000204679.8:c.270C= ENSP00000204679.4:p.Thr90=
ENST00000526820.5:c.*172C= ENSP00000434413.1:n.*172C=
ENST00000527076.1:n.1286C=
ENST00000527168.5:n.306C=
ENST00000529110.1:c.337C=
ENST00000529957.5:n.369C=
NM_032520.4:c.270C= NP_115909.1:p.Thr90=
XM_017023782.1:c.318C= XP_016879271.1:p.Thr106=
XM_017023783.1:c.-91C= XP_016879272.1:n.-91C=
NM_032520.5:c.270C= MANE Select NP_115909.1:p.Thr90=