Canonical Allele Identifier: CA399726004
Gene: NAGS HGNC NCBI
PYY HGNC NCBI

Linked Data

dbSNP Id: rs2049093895
gnomAD v4: 17-44006530-T-A
MyVariant Identifiers: chr17:g.42083898T>A (hg19) chr17:g.44006530T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006530T>A , CM000679.2:g.44006530T>A GRCh38
NC_000017.10:g.42083898T>A , CM000679.1:g.42083898T>A GRCh37
NC_000017.9:g.39439424T>A NCBI36
NG_008106.1:g.6867T>A
NG_023338.1:g.2940A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.917T>A (NAGS) MANE Select ENSP00000293404.2:p.Val306Asp
ENST00000293404.7:c.917T>A (NAGS) ENSP00000293404.2:p.Val306Asp
ENST00000589767.1:c.824T>A (NAGS) ENSP00000465408.1:p.Val275Asp
ENST00000592915.1:n.192T>A (NAGS)
NM_153006.2:c.917T>A (NAGS) NP_694551.1:p.Val306Asp
XM_011524438.1:c.917T>A (NAGS) XP_011522740.1:p.Val306Asp
XM_011524439.1:c.419T>A (NAGS) XP_011522741.1:p.Val140Asp
XM_011525035.1:c.-463+17042A>T (PYY) XP_011523337.1:n.-463+17042A>T
XM_011524439.2:c.419T>A (NAGS) XP_011522741.1:p.Val140Asp
NM_153006.3:c.917T>A (NAGS) MANE Select NP_694551.1:p.Val306Asp
Search 100 bp 5'
Search 100 bp 3'