Canonical Allele Identifier: CA2201614122
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1361902C= , CM000678.2:g.1361902C= GRCh38
NC_000016.9:g.1411903C= , CM000678.1:g.1411903C= GRCh37
NC_000016.8:g.1351904C= NCBI36
NG_016985.1:g.15004C=
NG_033129.1:g.57803G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.363C=
ENST00000529110.2:c.348C= ENSP00000435349.2:p.Asn116=
ENST00000529957.6:n.322C=
ENST00000683366.1:c.209C= ENSP00000507283.1:p.Thr70=
ENST00000683887.1:c.312C= ENSP00000506886.1:p.Asn104=
ENST00000684100.1:n.258C=
ENST00000684126.1:n.322C=
ENST00000684688.1:n.889C=
ENST00000204679.9:c.264C= MANE Select ENSP00000204679.4:p.Asn88=
ENST00000204679.8:c.264C= ENSP00000204679.4:p.Asn88=
ENST00000526820.5:c.*166C= ENSP00000434413.1:n.*166C=
ENST00000527076.1:n.1280C=
ENST00000527168.5:n.300C=
ENST00000529110.1:c.331C=
ENST00000529957.5:n.363C=
NM_032520.4:c.264C= NP_115909.1:p.Asn88=
XM_017023782.1:c.312C= XP_016879271.1:p.Asn104=
XM_017023783.1:c.-97C= XP_016879272.1:n.-97C=
NM_032520.5:c.264C= MANE Select NP_115909.1:p.Asn88=