Canonical Allele Identifier: CA500616058

Gene: NAGS PYY

Linked Data

• MyVariant Identifiers: chr17:g.42083476G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006108G>T , CM000679.2:g.44006108G>T	GRCh38
NC_000017.10:g.42083476G>T , CM000679.1:g.42083476G>T	GRCh37
NC_000017.9:g.39439002G>T	NCBI36
NG_008106.1:g.6445G>T
NG_023338.1:g.3362C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.786G>T (NAGS) MANE Select	ENSP00000293404.2:p.Gly262=
ENST00000293404.7:c.786G>T (NAGS)	ENSP00000293404.2:p.Gly262=
ENST00000589767.1:c.693G>T (NAGS)	ENSP00000465408.1:p.Gly231=
ENST00000592915.1:n.61G>T (NAGS)
NM_153006.2:c.786G>T (NAGS)	NP_694551.1:p.Gly262=
XM_011524438.1:c.786G>T (NAGS)	XP_011522740.1:p.Gly262=
XM_011524439.1:c.288G>T (NAGS)	XP_011522741.1:p.Gly96=
XM_011525035.1:c.-463+17464C>A (PYY)	XP_011523337.1:n.-463+17464C>A
XM_011524439.2:c.288G>T (NAGS)	XP_011522741.1:p.Gly96=
NM_153006.3:c.786G>T (NAGS) MANE Select	NP_694551.1:p.Gly262=