Canonical Allele Identifier: CA399725347

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006046G>A , CM000679.2:g.44006046G>A GRCh38
NC_000017.10:g.42083414G>A , CM000679.1:g.42083414G>A GRCh37
NC_000017.9:g.39438940G>A NCBI36
NG_008106.1:g.6383G>A
NG_023338.1:g.3424C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.724G>A (NAGS) MANE Select ENSP00000293404.2:p.Glu242Lys
ENST00000293404.7:c.724G>A (NAGS) ENSP00000293404.2:p.Glu242Lys
ENST00000589767.1:c.631G>A (NAGS) ENSP00000465408.1:p.Glu211Lys
NM_153006.2:c.724G>A (NAGS) NP_694551.1:p.Glu242Lys
XM_011524438.1:c.724G>A (NAGS) XP_011522740.1:p.Glu242Lys
XM_011524439.1:c.226G>A (NAGS) XP_011522741.1:p.Glu76Lys
XM_011525035.1:c.-463+17526C>T (PYY) XP_011523337.1:n.-463+17526C>T
XM_011524439.2:c.226G>A (NAGS) XP_011522741.1:p.Glu76Lys
NM_153006.3:c.724G>A (NAGS) MANE Select NP_694551.1:p.Glu242Lys