Canonical Allele Identifier: CA2201615290
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362648C= , CM000678.2:g.1362648C= GRCh38
NC_000016.9:g.1412649C= , CM000678.1:g.1412649C= GRCh37
NC_000016.8:g.1352650C= NCBI36
NG_016985.1:g.15750C=
NG_033129.1:g.57057G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.746C=
ENST00000529110.2:c.731C= ENSP00000435349.2:p.Ala244=
ENST00000529957.6:n.705C=
ENST00000683366.1:c.*379C= ENSP00000507283.1:n.*379C=
ENST00000683887.1:c.695C= ENSP00000506886.1:p.Ala232=
ENST00000684100.1:n.641C=
ENST00000684126.1:n.781C=
ENST00000684688.1:n.1272C=
ENST00000204679.9:c.647C= MANE Select ENSP00000204679.4:p.Ala216=
ENST00000204679.8:c.647C= ENSP00000204679.4:p.Ala216=
ENST00000527076.1:n.1870C=
ENST00000527168.5:n.814C=
ENST00000529957.5:n.746C=
NM_032520.4:c.647C= NP_115909.1:p.Ala216=
XM_017023782.1:c.695C= XP_016879271.1:p.Ala232=
XM_017023783.1:c.287C= XP_016879272.1:p.Ala96=
NM_032520.5:c.647C= MANE Select NP_115909.1:p.Ala216=