Canonical Allele Identifier: CA2261182209

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006601C= , CM000679.2:g.44006601C=	GRCh38
NC_000017.10:g.42083969C= , CM000679.1:g.42083969C=	GRCh37
NC_000017.9:g.39439495C=	NCBI36
NG_008106.1:g.6938C=
NG_023338.1:g.2869G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000293404.8:c.988C= (NAGS) MANE Select	ENSP00000293404.2:p.Arg330=
ENST00000293404.7:c.988C= (NAGS)	ENSP00000293404.2:p.Arg330=
ENST00000589767.1:c.895C= (NAGS)	ENSP00000465408.1:p.Arg299=
ENST00000592915.1:n.263C= (NAGS)
NM_153006.2:c.988C= (NAGS)	NP_694551.1:p.Arg330=
XM_011524438.1:c.988C= (NAGS)	XP_011522740.1:p.Arg330=
XM_011524439.1:c.490C= (NAGS)	XP_011522741.1:p.Arg164=
XM_011525035.1:c.-463+16971G= (PYY)	XP_011523337.1:n.-463+16971G=
XM_011524439.2:c.490C= (NAGS)	XP_011522741.1:p.Arg164=
NM_153006.3:c.988C= (NAGS) MANE Select	NP_694551.1:p.Arg330=