Canonical Allele Identifier: CA8595397

Linked Data

dbSNP Id: rs771090802

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007773G>T , CM000679.2:g.44007773G>T GRCh38
NC_000017.10:g.42085141G>T , CM000679.1:g.42085141G>T GRCh37
NC_000017.9:g.39440667G>T NCBI36
NG_008106.1:g.8110G>T
NG_023338.1:g.1697C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1451G>T (NAGS) MANE Select ENSP00000293404.2:p.Trp484Leu
ENST00000293404.7:c.1451G>T (NAGS) ENSP00000293404.2:p.Trp484Leu
ENST00000589767.1:c.1382G>T (NAGS) ENSP00000465408.1:p.Trp461Leu
ENST00000592915.1:n.1339G>T (NAGS)
NM_153006.2:c.1451G>T (NAGS) NP_694551.1:p.Trp484Leu
XM_011524438.1:c.1268+279G>T (NAGS) XP_011522740.1:n.1268+279G>T
XM_011524439.1:c.953G>T (NAGS) XP_011522741.1:p.Trp318Leu
XM_011525035.1:c.-463+15799C>A (PYY) XP_011523337.1:n.-463+15799C>A
XM_011524439.2:c.953G>T (NAGS) XP_011522741.1:p.Trp318Leu
NM_153006.3:c.1451G>T (NAGS) MANE Select NP_694551.1:p.Trp484Leu