Canonical Allele Identifier: CA8595289

Linked Data

dbSNP Id: rs759371794

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006607C>G , CM000679.2:g.44006607C>G GRCh38
NC_000017.10:g.42083975C>G , CM000679.1:g.42083975C>G GRCh37
NC_000017.9:g.39439501C>G NCBI36
NG_008106.1:g.6944C>G
NG_023338.1:g.2863G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.994C>G (NAGS) MANE Select ENSP00000293404.2:p.Gln332Glu
ENST00000293404.7:c.994C>G (NAGS) ENSP00000293404.2:p.Gln332Glu
ENST00000589767.1:c.901C>G (NAGS) ENSP00000465408.1:p.Gln301Glu
ENST00000592915.1:n.269C>G (NAGS)
NM_153006.2:c.994C>G (NAGS) NP_694551.1:p.Gln332Glu
XM_011524438.1:c.994C>G (NAGS) XP_011522740.1:p.Gln332Glu
XM_011524439.1:c.496C>G (NAGS) XP_011522741.1:p.Gln166Glu
XM_011525035.1:c.-463+16965G>C (PYY) XP_011523337.1:n.-463+16965G>C
XM_011524439.2:c.496C>G (NAGS) XP_011522741.1:p.Gln166Glu
NM_153006.3:c.994C>G (NAGS) MANE Select NP_694551.1:p.Gln332Glu