Canonical Allele Identifier: CA399725314

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006026A>G , CM000679.2:g.44006026A>G GRCh38
NC_000017.10:g.42083394A>G , CM000679.1:g.42083394A>G GRCh37
NC_000017.9:g.39438920A>G NCBI36
NG_008106.1:g.6363A>G
NG_023338.1:g.3444T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.704A>G (NAGS) MANE Select ENSP00000293404.2:p.Tyr235Cys
ENST00000293404.7:c.704A>G (NAGS) ENSP00000293404.2:p.Tyr235Cys
ENST00000589767.1:c.611A>G (NAGS) ENSP00000465408.1:p.Tyr204Cys
NM_153006.2:c.704A>G (NAGS) NP_694551.1:p.Tyr235Cys
XM_011524438.1:c.704A>G (NAGS) XP_011522740.1:p.Tyr235Cys
XM_011524439.1:c.206A>G (NAGS) XP_011522741.1:p.Tyr69Cys
XM_011525035.1:c.-463+17546T>C (PYY) XP_011523337.1:n.-463+17546T>C
XM_011524439.2:c.206A>G (NAGS) XP_011522741.1:p.Tyr69Cys
NM_153006.3:c.704A>G (NAGS) MANE Select NP_694551.1:p.Tyr235Cys