Canonical Allele Identifier: CA8595229

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs375437238
• ExAC: 17:42083507 G / A
• gnomAD v2: 17-42083507-G-A
• gnomAD v3: 17-44006139-G-A
• gnomAD v4: 17-44006139-G-A
• MyVariant Identifiers: chr17:g.42083507G>A (hg19) ; chr17:g.44006139G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006139G>A , CM000679.2:g.44006139G>A	GRCh38
NC_000017.10:g.42083507G>A , CM000679.1:g.42083507G>A	GRCh37
NC_000017.9:g.39439033G>A	NCBI36
NG_008106.1:g.6476G>A
NG_023338.1:g.3331C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.817G>A (NAGS) MANE Select	ENSP00000293404.2:p.Asp273Asn
ENST00000293404.7:c.817G>A (NAGS)	ENSP00000293404.2:p.Asp273Asn
ENST00000589767.1:c.724G>A (NAGS)	ENSP00000465408.1:p.Asp242Asn
ENST00000592915.1:n.92G>A (NAGS)
NM_153006.2:c.817G>A (NAGS)	NP_694551.1:p.Asp273Asn
XM_011524438.1:c.817G>A (NAGS)	XP_011522740.1:p.Asp273Asn
XM_011524439.1:c.319G>A (NAGS)	XP_011522741.1:p.Asp107Asn
XM_011525035.1:c.-463+17433C>T (PYY)	XP_011523337.1:n.-463+17433C>T
XM_011524439.2:c.319G>A (NAGS)	XP_011522741.1:p.Asp107Asn
NM_153006.3:c.817G>A (NAGS) MANE Select	NP_694551.1:p.Asp273Asn