Canonical Allele Identifier: CA399725331

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs763889856
• MyVariant Identifiers: chr17:g.42083403T>A (hg19) ; chr17:g.44006035T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006035T>A , CM000679.2:g.44006035T>A	GRCh38
NC_000017.10:g.42083403T>A , CM000679.1:g.42083403T>A	GRCh37
NC_000017.9:g.39438929T>A	NCBI36
NG_008106.1:g.6372T>A
NG_023338.1:g.3435A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.713T>A (NAGS) MANE Select	ENSP00000293404.2:p.Ile238Asn
ENST00000293404.7:c.713T>A (NAGS)	ENSP00000293404.2:p.Ile238Asn
ENST00000589767.1:c.620T>A (NAGS)	ENSP00000465408.1:p.Ile207Asn
NM_153006.2:c.713T>A (NAGS)	NP_694551.1:p.Ile238Asn
XM_011524438.1:c.713T>A (NAGS)	XP_011522740.1:p.Ile238Asn
XM_011524439.1:c.215T>A (NAGS)	XP_011522741.1:p.Ile72Asn
XM_011525035.1:c.-463+17537A>T (PYY)	XP_011523337.1:n.-463+17537A>T
XM_011524439.2:c.215T>A (NAGS)	XP_011522741.1:p.Ile72Asn
NM_153006.3:c.713T>A (NAGS) MANE Select	NP_694551.1:p.Ile238Asn