Canonical Allele Identifier: CA2261181956

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006106G= , CM000679.2:g.44006106G=	GRCh38
NC_000017.10:g.42083474G= , CM000679.1:g.42083474G=	GRCh37
NC_000017.9:g.39439000G=	NCBI36
NG_008106.1:g.6443G=
NG_023338.1:g.3364C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.784G= (NAGS) MANE Select	ENSP00000293404.2:p.Gly262=
ENST00000293404.7:c.784G= (NAGS)	ENSP00000293404.2:p.Gly262=
ENST00000589767.1:c.691G= (NAGS)	ENSP00000465408.1:p.Gly231=
ENST00000592915.1:n.59G= (NAGS)
NM_153006.2:c.784G= (NAGS)	NP_694551.1:p.Gly262=
XM_011524438.1:c.784G= (NAGS)	XP_011522740.1:p.Gly262=
XM_011524439.1:c.286G= (NAGS)	XP_011522741.1:p.Gly96=
XM_011525035.1:c.-463+17466C= (PYY)	XP_011523337.1:n.-463+17466C=
XM_011524439.2:c.286G= (NAGS)	XP_011522741.1:p.Gly96=
NM_153006.3:c.784G= (NAGS) MANE Select	NP_694551.1:p.Gly262=