Canonical Allele Identifier: CA2261182939

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007902G= , CM000679.2:g.44007902G=	GRCh38
NC_000017.10:g.42085270G= , CM000679.1:g.42085270G=	GRCh37
NC_000017.9:g.39440796G=	NCBI36
NG_008106.1:g.8239G=
NG_023338.1:g.1568C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1451+129G= (NAGS) MANE Select	ENSP00000293404.2:n.1451+129G=
ENST00000293404.7:c.1451+129G= (NAGS)	ENSP00000293404.2:n.1451+129G=
ENST00000589767.1:c.1382+129G= (NAGS)	ENSP00000465408.1:n.1382+129G=
ENST00000592915.1:n.1339+129G= (NAGS)
NM_153006.2:c.1451+129G= (NAGS)	NP_694551.1:n.1451+129G=
XM_011524438.1:c.1268+408G= (NAGS)	XP_011522740.1:n.1268+408G=
XM_011524439.1:c.953+129G= (NAGS)	XP_011522741.1:n.953+129G=
XM_011525035.1:c.-463+15670C= (PYY)	XP_011523337.1:n.-463+15670C=
XM_011524439.2:c.953+129G= (NAGS)	XP_011522741.1:n.953+129G=
NM_153006.3:c.1451+129G= (NAGS) MANE Select	NP_694551.1:n.1451+129G=