Canonical Allele Identifier: CA2261182898

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007801C= , CM000679.2:g.44007801C=	GRCh38
NC_000017.10:g.42085169C= , CM000679.1:g.42085169C=	GRCh37
NC_000017.9:g.39440695C=	NCBI36
NG_008106.1:g.8138C=
NG_023338.1:g.1669G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1451+28C= (NAGS) MANE Select	ENSP00000293404.2:n.1451+28C=
ENST00000293404.7:c.1451+28C= (NAGS)	ENSP00000293404.2:n.1451+28C=
ENST00000589767.1:c.1382+28C= (NAGS)	ENSP00000465408.1:n.1382+28C=
ENST00000592915.1:n.1339+28C= (NAGS)
NM_153006.2:c.1451+28C= (NAGS)	NP_694551.1:n.1451+28C=
XM_011524438.1:c.1268+307C= (NAGS)	XP_011522740.1:n.1268+307C=
XM_011524439.1:c.953+28C= (NAGS)	XP_011522741.1:n.953+28C=
XM_011525035.1:c.-463+15771G= (PYY)	XP_011523337.1:n.-463+15771G=
XM_011524439.2:c.953+28C= (NAGS)	XP_011522741.1:n.953+28C=
NM_153006.3:c.1451+28C= (NAGS) MANE Select	NP_694551.1:n.1451+28C=