Canonical Allele Identifier: CA399727746

Gene: NAGS PYY

Linked Data

• gnomAD v4: 17-44007672-C-A
• MyVariant Identifiers: chr17:g.42085040C>A (hg19) ; chr17:g.44007672C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007672C>A , CM000679.2:g.44007672C>A	GRCh38
NC_000017.10:g.42085040C>A , CM000679.1:g.42085040C>A	GRCh37
NC_000017.9:g.39440566C>A	NCBI36
NG_008106.1:g.8009C>A
NG_023338.1:g.1798G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000293404.8:c.1350C>A (NAGS) MANE Select	ENSP00000293404.2:p.Ser450Arg
ENST00000293404.7:c.1350C>A (NAGS)	ENSP00000293404.2:p.Ser450Arg
ENST00000589767.1:c.1281C>A (NAGS)	ENSP00000465408.1:p.Ser427Arg
ENST00000592915.1:n.1238C>A (NAGS)
NM_153006.2:c.1350C>A (NAGS)	NP_694551.1:p.Ser450Arg
XM_011524438.1:c.1268+178C>A (NAGS)	XP_011522740.1:n.1268+178C>A
XM_011524439.1:c.852C>A (NAGS)	XP_011522741.1:p.Ser284Arg
XM_011525035.1:c.-463+15900G>T (PYY)	XP_011523337.1:n.-463+15900G>T
XM_011524439.2:c.852C>A (NAGS)	XP_011522741.1:p.Ser284Arg
NM_153006.3:c.1350C>A (NAGS) MANE Select	NP_694551.1:p.Ser450Arg