Canonical Allele Identifier: CA2261182895

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007797T= , CM000679.2:g.44007797T=	GRCh38
NC_000017.10:g.42085165T= , CM000679.1:g.42085165T=	GRCh37
NC_000017.9:g.39440691T=	NCBI36
NG_008106.1:g.8134T=
NG_023338.1:g.1673A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1451+24T= (NAGS) MANE Select	ENSP00000293404.2:n.1451+24T=
ENST00000293404.7:c.1451+24T= (NAGS)	ENSP00000293404.2:n.1451+24T=
ENST00000589767.1:c.1382+24T= (NAGS)	ENSP00000465408.1:n.1382+24T=
ENST00000592915.1:n.1339+24T= (NAGS)
NM_153006.2:c.1451+24T= (NAGS)	NP_694551.1:n.1451+24T=
XM_011524438.1:c.1268+303T= (NAGS)	XP_011522740.1:n.1268+303T=
XM_011524439.1:c.953+24T= (NAGS)	XP_011522741.1:n.953+24T=
XM_011525035.1:c.-463+15775A= (PYY)	XP_011523337.1:n.-463+15775A=
XM_011524439.2:c.953+24T= (NAGS)	XP_011522741.1:n.953+24T=
NM_153006.3:c.1451+24T= (NAGS) MANE Select	NP_694551.1:n.1451+24T=