Canonical Allele Identifier: CA399726312
Gene: NAGS HGNC NCBI
PYY HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42083993G>A (hg19) chr17:g.44006625G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006625G>A , CM000679.2:g.44006625G>A GRCh38
NC_000017.10:g.42083993G>A , CM000679.1:g.42083993G>A GRCh37
NC_000017.9:g.39439519G>A NCBI36
NG_008106.1:g.6962G>A
NG_023338.1:g.2845C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.1012G>A (NAGS) MANE Select ENSP00000293404.2:p.Asp338Asn
ENST00000293404.7:c.1012G>A (NAGS) ENSP00000293404.2:p.Asp338Asn
ENST00000589767.1:c.919G>A (NAGS) ENSP00000465408.1:p.Asp307Asn
ENST00000592915.1:n.287G>A (NAGS)
NM_153006.2:c.1012G>A (NAGS) NP_694551.1:p.Asp338Asn
XM_011524438.1:c.1012G>A (NAGS) XP_011522740.1:p.Asp338Asn
XM_011524439.1:c.514G>A (NAGS) XP_011522741.1:p.Asp172Asn
XM_011525035.1:c.-463+16947C>T (PYY) XP_011523337.1:n.-463+16947C>T
XM_011524439.2:c.514G>A (NAGS) XP_011522741.1:p.Asp172Asn
NM_153006.3:c.1012G>A (NAGS) MANE Select NP_694551.1:p.Asp338Asn
Search 100 bp 5'
Search 100 bp 3'