Canonical Allele Identifier: CA399727783

Gene: NAGS PYY

Linked Data

• gnomAD v4: 17-44007680-G-A
• MyVariant Identifiers: chr17:g.42085048G>A (hg19) ; chr17:g.44007680G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007680G>A , CM000679.2:g.44007680G>A	GRCh38
NC_000017.10:g.42085048G>A , CM000679.1:g.42085048G>A	GRCh37
NC_000017.9:g.39440574G>A	NCBI36
NG_008106.1:g.8017G>A
NG_023338.1:g.1790C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000293404.8:c.1358G>A (NAGS) MANE Select	ENSP00000293404.2:p.Gly453Asp
ENST00000293404.7:c.1358G>A (NAGS)	ENSP00000293404.2:p.Gly453Asp
ENST00000589767.1:c.1289G>A (NAGS)	ENSP00000465408.1:p.Gly430Asp
ENST00000592915.1:n.1246G>A (NAGS)
NM_153006.2:c.1358G>A (NAGS)	NP_694551.1:p.Gly453Asp
XM_011524438.1:c.1268+186G>A (NAGS)	XP_011522740.1:n.1268+186G>A
XM_011524439.1:c.860G>A (NAGS)	XP_011522741.1:p.Gly287Asp
XM_011525035.1:c.-463+15892C>T (PYY)	XP_011523337.1:n.-463+15892C>T
XM_011524439.2:c.860G>A (NAGS)	XP_011522741.1:p.Gly287Asp
NM_153006.3:c.1358G>A (NAGS) MANE Select	NP_694551.1:p.Gly453Asp