Canonical Allele Identifier: CA399725618

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006142T>G , CM000679.2:g.44006142T>G GRCh38
NC_000017.10:g.42083510T>G , CM000679.1:g.42083510T>G GRCh37
NC_000017.9:g.39439036T>G NCBI36
NG_008106.1:g.6479T>G
NG_023338.1:g.3328A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.820T>G (NAGS) MANE Select ENSP00000293404.2:p.Ser274Ala
ENST00000293404.7:c.820T>G (NAGS) ENSP00000293404.2:p.Ser274Ala
ENST00000589767.1:c.727T>G (NAGS) ENSP00000465408.1:p.Ser243Ala
ENST00000592915.1:n.95T>G (NAGS)
NM_153006.2:c.820T>G (NAGS) NP_694551.1:p.Ser274Ala
XM_011524438.1:c.820T>G (NAGS) XP_011522740.1:p.Ser274Ala
XM_011524439.1:c.322T>G (NAGS) XP_011522741.1:p.Ser108Ala
XM_011525035.1:c.-463+17430A>C (PYY) XP_011523337.1:n.-463+17430A>C
XM_011524439.2:c.322T>G (NAGS) XP_011522741.1:p.Ser108Ala
NM_153006.3:c.820T>G (NAGS) MANE Select NP_694551.1:p.Ser274Ala