Canonical Allele Identifier: CA2261182842

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007721G= , CM000679.2:g.44007721G=	GRCh38
NC_000017.10:g.42085089G= , CM000679.1:g.42085089G=	GRCh37
NC_000017.9:g.39440615G=	NCBI36
NG_008106.1:g.8058G=
NG_023338.1:g.1749C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1399G= (NAGS) MANE Select	ENSP00000293404.2:p.Asp467=
ENST00000293404.7:c.1399G= (NAGS)	ENSP00000293404.2:p.Asp467=
ENST00000589767.1:c.1330G= (NAGS)	ENSP00000465408.1:p.Asp444=
ENST00000592915.1:n.1287G= (NAGS)
NM_153006.2:c.1399G= (NAGS)	NP_694551.1:p.Asp467=
XM_011524438.1:c.1268+227G= (NAGS)	XP_011522740.1:n.1268+227G=
XM_011524439.1:c.901G= (NAGS)	XP_011522741.1:p.Asp301=
XM_011525035.1:c.-463+15851C= (PYY)	XP_011523337.1:n.-463+15851C=
XM_011524439.2:c.901G= (NAGS)	XP_011522741.1:p.Asp301=
NM_153006.3:c.1399G= (NAGS) MANE Select	NP_694551.1:p.Asp467=