Canonical Allele Identifier: CA2261182092

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006395A= , CM000679.2:g.44006395A=	GRCh38
NC_000017.10:g.42083763A= , CM000679.1:g.42083763A=	GRCh37
NC_000017.9:g.39439289A=	NCBI36
NG_008106.1:g.6732A=
NG_023338.1:g.3075T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000293404.8:c.916-134A= (NAGS) MANE Select	ENSP00000293404.2:n.916-134A=
ENST00000293404.7:c.916-134A= (NAGS)	ENSP00000293404.2:n.916-134A=
ENST00000589767.1:c.823-134A= (NAGS)	ENSP00000465408.1:n.823-134A=
ENST00000592915.1:n.191-134A= (NAGS)
NM_153006.2:c.916-134A= (NAGS)	NP_694551.1:n.916-134A=
XM_011524438.1:c.916-134A= (NAGS)	XP_011522740.1:n.916-134A=
XM_011524439.1:c.418-134A= (NAGS)	XP_011522741.1:n.418-134A=
XM_011525035.1:c.-463+17177T= (PYY)	XP_011523337.1:n.-463+17177T=
XM_011524439.2:c.418-134A= (NAGS)	XP_011522741.1:n.418-134A=
NM_153006.3:c.916-134A= (NAGS) MANE Select	NP_694551.1:n.916-134A=