Canonical Allele Identifier: CA2261182845

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007725T= , CM000679.2:g.44007725T=	GRCh38
NC_000017.10:g.42085093T= , CM000679.1:g.42085093T=	GRCh37
NC_000017.9:g.39440619T=	NCBI36
NG_008106.1:g.8062T=
NG_023338.1:g.1745A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1403T= (NAGS) MANE Select	ENSP00000293404.2:p.Leu468=
ENST00000293404.7:c.1403T= (NAGS)	ENSP00000293404.2:p.Leu468=
ENST00000589767.1:c.1334T= (NAGS)	ENSP00000465408.1:p.Leu445=
ENST00000592915.1:n.1291T= (NAGS)
NM_153006.2:c.1403T= (NAGS)	NP_694551.1:p.Leu468=
XM_011524438.1:c.1268+231T= (NAGS)	XP_011522740.1:n.1268+231T=
XM_011524439.1:c.905T= (NAGS)	XP_011522741.1:p.Leu302=
XM_011525035.1:c.-463+15847A= (PYY)	XP_011523337.1:n.-463+15847A=
XM_011524439.2:c.905T= (NAGS)	XP_011522741.1:p.Leu302=
NM_153006.3:c.1403T= (NAGS) MANE Select	NP_694551.1:p.Leu468=