Canonical Allele Identifier: CA399726266
Gene: NAGS HGNC NCBI
PYY HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42083977G>C (hg19) chr17:g.44006609G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006609G>C , CM000679.2:g.44006609G>C GRCh38
NC_000017.10:g.42083977G>C , CM000679.1:g.42083977G>C GRCh37
NC_000017.9:g.39439503G>C NCBI36
NG_008106.1:g.6946G>C
NG_023338.1:g.2861C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.996G>C (NAGS) MANE Select ENSP00000293404.2:p.Gln332His
ENST00000293404.7:c.996G>C (NAGS) ENSP00000293404.2:p.Gln332His
ENST00000589767.1:c.903G>C (NAGS) ENSP00000465408.1:p.Gln301His
ENST00000592915.1:n.271G>C (NAGS)
NM_153006.2:c.996G>C (NAGS) NP_694551.1:p.Gln332His
XM_011524438.1:c.996G>C (NAGS) XP_011522740.1:p.Gln332His
XM_011524439.1:c.498G>C (NAGS) XP_011522741.1:p.Gln166His
XM_011525035.1:c.-463+16963C>G (PYY) XP_011523337.1:n.-463+16963C>G
XM_011524439.2:c.498G>C (NAGS) XP_011522741.1:p.Gln166His
NM_153006.3:c.996G>C (NAGS) MANE Select NP_694551.1:p.Gln332His
Search 100 bp 5'
Search 100 bp 3'