Canonical Allele Identifier: CA399727787

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007680G>T , CM000679.2:g.44007680G>T GRCh38
NC_000017.10:g.42085048G>T , CM000679.1:g.42085048G>T GRCh37
NC_000017.9:g.39440574G>T NCBI36
NG_008106.1:g.8017G>T
NG_023338.1:g.1790C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1358G>T (NAGS) MANE Select ENSP00000293404.2:p.Gly453Val
ENST00000293404.7:c.1358G>T (NAGS) ENSP00000293404.2:p.Gly453Val
ENST00000589767.1:c.1289G>T (NAGS) ENSP00000465408.1:p.Gly430Val
ENST00000592915.1:n.1246G>T (NAGS)
NM_153006.2:c.1358G>T (NAGS) NP_694551.1:p.Gly453Val
XM_011524438.1:c.1268+186G>T (NAGS) XP_011522740.1:n.1268+186G>T
XM_011524439.1:c.860G>T (NAGS) XP_011522741.1:p.Gly287Val
XM_011525035.1:c.-463+15892C>A (PYY) XP_011523337.1:n.-463+15892C>A
XM_011524439.2:c.860G>T (NAGS) XP_011522741.1:p.Gly287Val
NM_153006.3:c.1358G>T (NAGS) MANE Select NP_694551.1:p.Gly453Val