Canonical Allele Identifier: CA2261182840

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007719G= , CM000679.2:g.44007719G=	GRCh38
NC_000017.10:g.42085087G= , CM000679.1:g.42085087G=	GRCh37
NC_000017.9:g.39440613G=	NCBI36
NG_008106.1:g.8056G=
NG_023338.1:g.1751C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1397G= (NAGS) MANE Select	ENSP00000293404.2:p.Arg466=
ENST00000293404.7:c.1397G= (NAGS)	ENSP00000293404.2:p.Arg466=
ENST00000589767.1:c.1328G= (NAGS)	ENSP00000465408.1:p.Arg443=
ENST00000592915.1:n.1285G= (NAGS)
NM_153006.2:c.1397G= (NAGS)	NP_694551.1:p.Arg466=
XM_011524438.1:c.1268+225G= (NAGS)	XP_011522740.1:n.1268+225G=
XM_011524439.1:c.899G= (NAGS)	XP_011522741.1:p.Arg300=
XM_011525035.1:c.-463+15853C= (PYY)	XP_011523337.1:n.-463+15853C=
XM_011524439.2:c.899G= (NAGS)	XP_011522741.1:p.Arg300=
NM_153006.3:c.1397G= (NAGS) MANE Select	NP_694551.1:p.Arg466=