Canonical Allele Identifier: CA399726027
Gene: NAGS HGNC NCBI
PYY HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42083907A>C (hg19) chr17:g.44006539A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006539A>C , CM000679.2:g.44006539A>C GRCh38
NC_000017.10:g.42083907A>C , CM000679.1:g.42083907A>C GRCh37
NC_000017.9:g.39439433A>C NCBI36
NG_008106.1:g.6876A>C
NG_023338.1:g.2931T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.926A>C (NAGS) MANE Select ENSP00000293404.2:p.Asn309Thr
ENST00000293404.7:c.926A>C (NAGS) ENSP00000293404.2:p.Asn309Thr
ENST00000589767.1:c.833A>C (NAGS) ENSP00000465408.1:p.Asn278Thr
ENST00000592915.1:n.201A>C (NAGS)
NM_153006.2:c.926A>C (NAGS) NP_694551.1:p.Asn309Thr
XM_011524438.1:c.926A>C (NAGS) XP_011522740.1:p.Asn309Thr
XM_011524439.1:c.428A>C (NAGS) XP_011522741.1:p.Asn143Thr
XM_011525035.1:c.-463+17033T>G (PYY) XP_011523337.1:n.-463+17033T>G
XM_011524439.2:c.428A>C (NAGS) XP_011522741.1:p.Asn143Thr
NM_153006.3:c.926A>C (NAGS) MANE Select NP_694551.1:p.Asn309Thr
Search 100 bp 5'
Search 100 bp 3'