Canonical Allele Identifier: CA399726025
Gene: NAGS HGNC NCBI
PYY HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42083906A>G (hg19) chr17:g.44006538A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006538A>G , CM000679.2:g.44006538A>G GRCh38
NC_000017.10:g.42083906A>G , CM000679.1:g.42083906A>G GRCh37
NC_000017.9:g.39439432A>G NCBI36
NG_008106.1:g.6875A>G
NG_023338.1:g.2932T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.925A>G (NAGS) MANE Select ENSP00000293404.2:p.Asn309Asp
ENST00000293404.7:c.925A>G (NAGS) ENSP00000293404.2:p.Asn309Asp
ENST00000589767.1:c.832A>G (NAGS) ENSP00000465408.1:p.Asn278Asp
ENST00000592915.1:n.200A>G (NAGS)
NM_153006.2:c.925A>G (NAGS) NP_694551.1:p.Asn309Asp
XM_011524438.1:c.925A>G (NAGS) XP_011522740.1:p.Asn309Asp
XM_011524439.1:c.427A>G (NAGS) XP_011522741.1:p.Asn143Asp
XM_011525035.1:c.-463+17034T>C (PYY) XP_011523337.1:n.-463+17034T>C
XM_011524439.2:c.427A>G (NAGS) XP_011522741.1:p.Asn143Asp
NM_153006.3:c.925A>G (NAGS) MANE Select NP_694551.1:p.Asn309Asp
Search 100 bp 5'
Search 100 bp 3'