Canonical Allele Identifier: CA399725379

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006061C>A , CM000679.2:g.44006061C>A GRCh38
NC_000017.10:g.42083429C>A , CM000679.1:g.42083429C>A GRCh37
NC_000017.9:g.39438955C>A NCBI36
NG_008106.1:g.6398C>A
NG_023338.1:g.3409G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.739C>A (NAGS) MANE Select ENSP00000293404.2:p.Gln247Lys
ENST00000293404.7:c.739C>A (NAGS) ENSP00000293404.2:p.Gln247Lys
ENST00000589767.1:c.646C>A (NAGS) ENSP00000465408.1:p.Gln216Lys
ENST00000592915.1:n.14C>A (NAGS)
NM_153006.2:c.739C>A (NAGS) NP_694551.1:p.Gln247Lys
XM_011524438.1:c.739C>A (NAGS) XP_011522740.1:p.Gln247Lys
XM_011524439.1:c.241C>A (NAGS) XP_011522741.1:p.Gln81Lys
XM_011525035.1:c.-463+17511G>T (PYY) XP_011523337.1:n.-463+17511G>T
XM_011524439.2:c.241C>A (NAGS) XP_011522741.1:p.Gln81Lys
NM_153006.3:c.739C>A (NAGS) MANE Select NP_694551.1:p.Gln247Lys