Canonical Allele Identifier: CA2261182861

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007754A= , CM000679.2:g.44007754A=	GRCh38
NC_000017.10:g.42085122A= , CM000679.1:g.42085122A=	GRCh37
NC_000017.9:g.39440648A=	NCBI36
NG_008106.1:g.8091A=
NG_023338.1:g.1716T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1432A= (NAGS) MANE Select	ENSP00000293404.2:p.Thr478=
ENST00000293404.7:c.1432A= (NAGS)	ENSP00000293404.2:p.Thr478=
ENST00000589767.1:c.1363A= (NAGS)	ENSP00000465408.1:p.Thr455=
ENST00000592915.1:n.1320A= (NAGS)
NM_153006.2:c.1432A= (NAGS)	NP_694551.1:p.Thr478=
XM_011524438.1:c.1268+260A= (NAGS)	XP_011522740.1:n.1268+260A=
XM_011524439.1:c.934A= (NAGS)	XP_011522741.1:p.Thr312=
XM_011525035.1:c.-463+15818T= (PYY)	XP_011523337.1:n.-463+15818T=
XM_011524439.2:c.934A= (NAGS)	XP_011522741.1:p.Thr312=
NM_153006.3:c.1432A= (NAGS) MANE Select	NP_694551.1:p.Thr478=