Canonical Allele Identifier: CA2201615193
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362528C= , CM000678.2:g.1362528C= GRCh38
NC_000016.9:g.1412529C= , CM000678.1:g.1412529C= GRCh37
NC_000016.8:g.1352530C= NCBI36
NG_016985.1:g.15630C=
NG_033129.1:g.57177G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.702C=
ENST00000529110.2:c.687C= ENSP00000435349.2:p.Thr229=
ENST00000529957.6:n.661C=
ENST00000683366.1:c.*335C= ENSP00000507283.1:n.*335C=
ENST00000683887.1:c.651C= ENSP00000506886.1:p.Thr217=
ENST00000684100.1:n.597C=
ENST00000684126.1:n.661C=
ENST00000684688.1:n.1228C=
ENST00000204679.9:c.603C= MANE Select ENSP00000204679.4:p.Thr201=
ENST00000204679.8:c.603C= ENSP00000204679.4:p.Thr201=
ENST00000527076.1:n.1750C=
ENST00000527168.5:n.770C=
ENST00000529957.5:n.702C=
NM_032520.4:c.603C= NP_115909.1:p.Thr201=
XM_017023782.1:c.651C= XP_016879271.1:p.Thr217=
XM_017023783.1:c.243C= XP_016879272.1:p.Thr81=
NM_032520.5:c.603C= MANE Select NP_115909.1:p.Thr201=