Canonical Allele Identifier: CA399726295
Gene: NAGS HGNC NCBI
PYY HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42083988T>A (hg19) chr17:g.44006620T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006620T>A , CM000679.2:g.44006620T>A GRCh38
NC_000017.10:g.42083988T>A , CM000679.1:g.42083988T>A GRCh37
NC_000017.9:g.39439514T>A NCBI36
NG_008106.1:g.6957T>A
NG_023338.1:g.2850A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.1007T>A (NAGS) MANE Select ENSP00000293404.2:p.Ile336Asn
ENST00000293404.7:c.1007T>A (NAGS) ENSP00000293404.2:p.Ile336Asn
ENST00000589767.1:c.914T>A (NAGS) ENSP00000465408.1:p.Ile305Asn
ENST00000592915.1:n.282T>A (NAGS)
NM_153006.2:c.1007T>A (NAGS) NP_694551.1:p.Ile336Asn
XM_011524438.1:c.1007T>A (NAGS) XP_011522740.1:p.Ile336Asn
XM_011524439.1:c.509T>A (NAGS) XP_011522741.1:p.Ile170Asn
XM_011525035.1:c.-463+16952A>T (PYY) XP_011523337.1:n.-463+16952A>T
XM_011524439.2:c.509T>A (NAGS) XP_011522741.1:p.Ile170Asn
NM_153006.3:c.1007T>A (NAGS) MANE Select NP_694551.1:p.Ile336Asn
Search 100 bp 5'
Search 100 bp 3'