Canonical Allele Identifier: CA2638146031
Gene: NAGS HGNC NCBI
PYY HGNC NCBI

Linked Data

gnomAD v4: 17-44005989-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44005989A>G , CM000679.2:g.44005989A>G GRCh38
NC_000017.10:g.42083357A>G , CM000679.1:g.42083357A>G GRCh37
NC_000017.9:g.39438883A>G NCBI36
NG_008106.1:g.6326A>G
NG_023338.1:g.3481T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.702-35A>G (NAGS) MANE Select ENSP00000293404.2:n.702-35A>G
ENST00000293404.7:c.702-35A>G (NAGS) ENSP00000293404.2:n.702-35A>G
ENST00000589767.1:c.609-35A>G (NAGS) ENSP00000465408.1:n.609-35A>G
NM_153006.2:c.702-35A>G (NAGS) NP_694551.1:n.702-35A>G
XM_011524438.1:c.702-35A>G (NAGS) XP_011522740.1:n.702-35A>G
XM_011524439.1:c.204-35A>G (NAGS) XP_011522741.1:n.204-35A>G
XM_011525035.1:c.-463+17583T>C (PYY) XP_011523337.1:n.-463+17583T>C
XM_011524439.2:c.204-35A>G (NAGS) XP_011522741.1:n.204-35A>G
NM_153006.3:c.702-35A>G (NAGS) MANE Select NP_694551.1:n.702-35A>G
Search 100 bp 5'
Search 100 bp 3'