Canonical Allele Identifier: CA2261182811

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007674G= , CM000679.2:g.44007674G= GRCh38
NC_000017.10:g.42085042G= , CM000679.1:g.42085042G= GRCh37
NC_000017.9:g.39440568G= NCBI36
NG_008106.1:g.8011G=
NG_023338.1:g.1796C=

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1352G= (NAGS) MANE Select ENSP00000293404.2:p.Arg451=
ENST00000293404.7:c.1352G= (NAGS) ENSP00000293404.2:p.Arg451=
ENST00000589767.1:c.1283G= (NAGS) ENSP00000465408.1:p.Arg428=
ENST00000592915.1:n.1240G= (NAGS)
NM_153006.2:c.1352G= (NAGS) NP_694551.1:p.Arg451=
XM_011524438.1:c.1268+180G= (NAGS) XP_011522740.1:n.1268+180G=
XM_011524439.1:c.854G= (NAGS) XP_011522741.1:p.Arg285=
XM_011525035.1:c.-463+15898C= (PYY) XP_011523337.1:n.-463+15898C=
XM_011524439.2:c.854G= (NAGS) XP_011522741.1:p.Arg285=
NM_153006.3:c.1352G= (NAGS) MANE Select NP_694551.1:p.Arg451=