Canonical Allele Identifier: CA2261182017

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006226A= , CM000679.2:g.44006226A= GRCh38
NC_000017.10:g.42083594A= , CM000679.1:g.42083594A= GRCh37
NC_000017.9:g.39439120A= NCBI36
NG_008106.1:g.6563A=
NG_023338.1:g.3244T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.904A= (NAGS) MANE Select ENSP00000293404.2:p.Ser302=
ENST00000293404.7:c.904A= (NAGS) ENSP00000293404.2:p.Ser302=
ENST00000589767.1:c.811A= (NAGS) ENSP00000465408.1:p.Ser271=
ENST00000592915.1:n.179A= (NAGS)
NM_153006.2:c.904A= (NAGS) NP_694551.1:p.Ser302=
XM_011524438.1:c.904A= (NAGS) XP_011522740.1:p.Ser302=
XM_011524439.1:c.406A= (NAGS) XP_011522741.1:p.Ser136=
XM_011525035.1:c.-463+17346T= (PYY) XP_011523337.1:n.-463+17346T=
XM_011524439.2:c.406A= (NAGS) XP_011522741.1:p.Ser136=
NM_153006.3:c.904A= (NAGS) MANE Select NP_694551.1:p.Ser302=