Canonical Allele Identifier: CA399725474

Gene: NAGS PYY

Linked Data

• MyVariant Identifiers: chr17:g.42083472T>G (hg19) ; chr17:g.44006104T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006104T>G , CM000679.2:g.44006104T>G	GRCh38
NC_000017.10:g.42083472T>G , CM000679.1:g.42083472T>G	GRCh37
NC_000017.9:g.39438998T>G	NCBI36
NG_008106.1:g.6441T>G
NG_023338.1:g.3366A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.782T>G (NAGS) MANE Select	ENSP00000293404.2:p.Ile261Ser
ENST00000293404.7:c.782T>G (NAGS)	ENSP00000293404.2:p.Ile261Ser
ENST00000589767.1:c.689T>G (NAGS)	ENSP00000465408.1:p.Ile230Ser
ENST00000592915.1:n.57T>G (NAGS)
NM_153006.2:c.782T>G (NAGS)	NP_694551.1:p.Ile261Ser
XM_011524438.1:c.782T>G (NAGS)	XP_011522740.1:p.Ile261Ser
XM_011524439.1:c.284T>G (NAGS)	XP_011522741.1:p.Ile95Ser
XM_011525035.1:c.-463+17468A>C (PYY)	XP_011523337.1:n.-463+17468A>C
XM_011524439.2:c.284T>G (NAGS)	XP_011522741.1:p.Ile95Ser
NM_153006.3:c.782T>G (NAGS) MANE Select	NP_694551.1:p.Ile261Ser