Canonical Allele Identifier: CA2261182863

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007757A= , CM000679.2:g.44007757A=	GRCh38
NC_000017.10:g.42085125A= , CM000679.1:g.42085125A=	GRCh37
NC_000017.9:g.39440651A=	NCBI36
NG_008106.1:g.8094A=
NG_023338.1:g.1713T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1435A= (NAGS) MANE Select	ENSP00000293404.2:p.Asn479=
ENST00000293404.7:c.1435A= (NAGS)	ENSP00000293404.2:p.Asn479=
ENST00000589767.1:c.1366A= (NAGS)	ENSP00000465408.1:p.Asn456=
ENST00000592915.1:n.1323A= (NAGS)
NM_153006.2:c.1435A= (NAGS)	NP_694551.1:p.Asn479=
XM_011524438.1:c.1268+263A= (NAGS)	XP_011522740.1:n.1268+263A=
XM_011524439.1:c.937A= (NAGS)	XP_011522741.1:p.Asn313=
XM_011525035.1:c.-463+15815T= (PYY)	XP_011523337.1:n.-463+15815T=
XM_011524439.2:c.937A= (NAGS)	XP_011522741.1:p.Asn313=
NM_153006.3:c.1435A= (NAGS) MANE Select	NP_694551.1:p.Asn479=