Canonical Allele Identifier: CA2201614117
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1361901A= , CM000678.2:g.1361901A= GRCh38
NC_000016.9:g.1411902A= , CM000678.1:g.1411902A= GRCh37
NC_000016.8:g.1351903A= NCBI36
NG_016985.1:g.15003A=
NG_033129.1:g.57804T=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.362A=
ENST00000529110.2:c.347A= ENSP00000435349.2:p.Asn116=
ENST00000529957.6:n.321A=
ENST00000683366.1:c.208A= ENSP00000507283.1:p.Thr70=
ENST00000683887.1:c.311A= ENSP00000506886.1:p.Asn104=
ENST00000684100.1:n.257A=
ENST00000684126.1:n.321A=
ENST00000684688.1:n.888A=
ENST00000204679.9:c.263A= MANE Select ENSP00000204679.4:p.Asn88=
ENST00000204679.8:c.263A= ENSP00000204679.4:p.Asn88=
ENST00000526820.5:c.*165A= ENSP00000434413.1:n.*165A=
ENST00000527076.1:n.1279A=
ENST00000527168.5:n.299A=
ENST00000529110.1:c.330A=
ENST00000529957.5:n.362A=
NM_032520.4:c.263A= NP_115909.1:p.Asn88=
XM_017023782.1:c.311A= XP_016879271.1:p.Asn104=
XM_017023783.1:c.-98A= XP_016879272.1:n.-98A=
NM_032520.5:c.263A= MANE Select NP_115909.1:p.Asn88=