Canonical Allele Identifier: CA2261181963

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006120G= , CM000679.2:g.44006120G=	GRCh38
NC_000017.10:g.42083488G= , CM000679.1:g.42083488G=	GRCh37
NC_000017.9:g.39439014G=	NCBI36
NG_008106.1:g.6457G=
NG_023338.1:g.3350C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.798G= (NAGS) MANE Select	ENSP00000293404.2:p.Ala266=
ENST00000293404.7:c.798G= (NAGS)	ENSP00000293404.2:p.Ala266=
ENST00000589767.1:c.705G= (NAGS)	ENSP00000465408.1:p.Ala235=
ENST00000592915.1:n.73G= (NAGS)
NM_153006.2:c.798G= (NAGS)	NP_694551.1:p.Ala266=
XM_011524438.1:c.798G= (NAGS)	XP_011522740.1:p.Ala266=
XM_011524439.1:c.300G= (NAGS)	XP_011522741.1:p.Ala100=
XM_011525035.1:c.-463+17452C= (PYY)	XP_011523337.1:n.-463+17452C=
XM_011524439.2:c.300G= (NAGS)	XP_011522741.1:p.Ala100=
NM_153006.3:c.798G= (NAGS) MANE Select	NP_694551.1:p.Ala266=