Canonical Allele Identifier: CA2261182927

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007875T= , CM000679.2:g.44007875T=	GRCh38
NC_000017.10:g.42085243T= , CM000679.1:g.42085243T=	GRCh37
NC_000017.9:g.39440769T=	NCBI36
NG_008106.1:g.8212T=
NG_023338.1:g.1595A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1451+102T= (NAGS) MANE Select	ENSP00000293404.2:n.1451+102T=
ENST00000293404.7:c.1451+102T= (NAGS)	ENSP00000293404.2:n.1451+102T=
ENST00000589767.1:c.1382+102T= (NAGS)	ENSP00000465408.1:n.1382+102T=
ENST00000592915.1:n.1339+102T= (NAGS)
NM_153006.2:c.1451+102T= (NAGS)	NP_694551.1:n.1451+102T=
XM_011524438.1:c.1268+381T= (NAGS)	XP_011522740.1:n.1268+381T=
XM_011524439.1:c.953+102T= (NAGS)	XP_011522741.1:n.953+102T=
XM_011525035.1:c.-463+15697A= (PYY)	XP_011523337.1:n.-463+15697A=
XM_011524439.2:c.953+102T= (NAGS)	XP_011522741.1:n.953+102T=
NM_153006.3:c.1451+102T= (NAGS) MANE Select	NP_694551.1:n.1451+102T=