Canonical Allele Identifier: CA399725433

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006085A>T , CM000679.2:g.44006085A>T GRCh38
NC_000017.10:g.42083453A>T , CM000679.1:g.42083453A>T GRCh37
NC_000017.9:g.39438979A>T NCBI36
NG_008106.1:g.6422A>T
NG_023338.1:g.3385T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.763A>T (NAGS) MANE Select ENSP00000293404.2:p.Ile255Phe
ENST00000293404.7:c.763A>T (NAGS) ENSP00000293404.2:p.Ile255Phe
ENST00000589767.1:c.670A>T (NAGS) ENSP00000465408.1:p.Ile224Phe
ENST00000592915.1:n.38A>T (NAGS)
NM_153006.2:c.763A>T (NAGS) NP_694551.1:p.Ile255Phe
XM_011524438.1:c.763A>T (NAGS) XP_011522740.1:p.Ile255Phe
XM_011524439.1:c.265A>T (NAGS) XP_011522741.1:p.Ile89Phe
XM_011525035.1:c.-463+17487T>A (PYY) XP_011523337.1:n.-463+17487T>A
XM_011524439.2:c.265A>T (NAGS) XP_011522741.1:p.Ile89Phe
NM_153006.3:c.763A>T (NAGS) MANE Select NP_694551.1:p.Ile255Phe