Canonical Allele Identifier: CA399726050
Gene: NAGS HGNC NCBI
PYY HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42083918C>G (hg19) chr17:g.44006550C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006550C>G , CM000679.2:g.44006550C>G GRCh38
NC_000017.10:g.42083918C>G , CM000679.1:g.42083918C>G GRCh37
NC_000017.9:g.39439444C>G NCBI36
NG_008106.1:g.6887C>G
NG_023338.1:g.2920G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.937C>G (NAGS) MANE Select ENSP00000293404.2:p.Pro313Ala
ENST00000293404.7:c.937C>G (NAGS) ENSP00000293404.2:p.Pro313Ala
ENST00000589767.1:c.844C>G (NAGS) ENSP00000465408.1:p.Pro282Ala
ENST00000592915.1:n.212C>G (NAGS)
NM_153006.2:c.937C>G (NAGS) NP_694551.1:p.Pro313Ala
XM_011524438.1:c.937C>G (NAGS) XP_011522740.1:p.Pro313Ala
XM_011524439.1:c.439C>G (NAGS) XP_011522741.1:p.Pro147Ala
XM_011525035.1:c.-463+17022G>C (PYY) XP_011523337.1:n.-463+17022G>C
XM_011524439.2:c.439C>G (NAGS) XP_011522741.1:p.Pro147Ala
NM_153006.3:c.937C>G (NAGS) MANE Select NP_694551.1:p.Pro313Ala
Search 100 bp 5'
Search 100 bp 3'