Canonical Allele Identifier: CA2261182816

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007684A= , CM000679.2:g.44007684A= GRCh38
NC_000017.10:g.42085052A= , CM000679.1:g.42085052A= GRCh37
NC_000017.9:g.39440578A= NCBI36
NG_008106.1:g.8021A=
NG_023338.1:g.1786T=

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1362A= (NAGS) MANE Select ENSP00000293404.2:p.Gln454=
ENST00000293404.7:c.1362A= (NAGS) ENSP00000293404.2:p.Gln454=
ENST00000589767.1:c.1293A= (NAGS) ENSP00000465408.1:p.Gln431=
ENST00000592915.1:n.1250A= (NAGS)
NM_153006.2:c.1362A= (NAGS) NP_694551.1:p.Gln454=
XM_011524438.1:c.1268+190A= (NAGS) XP_011522740.1:n.1268+190A=
XM_011524439.1:c.864A= (NAGS) XP_011522741.1:p.Gln288=
XM_011525035.1:c.-463+15888T= (PYY) XP_011523337.1:n.-463+15888T=
XM_011524439.2:c.864A= (NAGS) XP_011522741.1:p.Gln288=
NM_153006.3:c.1362A= (NAGS) MANE Select NP_694551.1:p.Gln454=