Canonical Allele Identifier: CA399725907

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006225C>G , CM000679.2:g.44006225C>G GRCh38
NC_000017.10:g.42083593C>G , CM000679.1:g.42083593C>G GRCh37
NC_000017.9:g.39439119C>G NCBI36
NG_008106.1:g.6562C>G
NG_023338.1:g.3245G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.903C>G (NAGS) MANE Select ENSP00000293404.2:p.Asp301Glu
ENST00000293404.7:c.903C>G (NAGS) ENSP00000293404.2:p.Asp301Glu
ENST00000589767.1:c.810C>G (NAGS) ENSP00000465408.1:p.Asp270Glu
ENST00000592915.1:n.178C>G (NAGS)
NM_153006.2:c.903C>G (NAGS) NP_694551.1:p.Asp301Glu
XM_011524438.1:c.903C>G (NAGS) XP_011522740.1:p.Asp301Glu
XM_011524439.1:c.405C>G (NAGS) XP_011522741.1:p.Asp135Glu
XM_011525035.1:c.-463+17347G>C (PYY) XP_011523337.1:n.-463+17347G>C
XM_011524439.2:c.405C>G (NAGS) XP_011522741.1:p.Asp135Glu
NM_153006.3:c.903C>G (NAGS) MANE Select NP_694551.1:p.Asp301Glu