Canonical Allele Identifier: CA8595176

Gene: NAGS PYY

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44005822A>G , CM000679.2:g.44005822A>G	GRCh38
NC_000017.10:g.42083190A>G , CM000679.1:g.42083190A>G	GRCh37
NC_000017.9:g.39438716A>G	NCBI36
NG_008106.1:g.6159A>G
NG_023338.1:g.3648T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.612A>G (NAGS) MANE Select	ENSP00000293404.2:p.Val204=
ENST00000293404.7:c.612A>G (NAGS)	ENSP00000293404.2:p.Val204=
ENST00000589767.1:c.519A>G (NAGS)	ENSP00000465408.1:p.Val173=
NM_153006.2:c.612A>G (NAGS)	NP_694551.1:p.Val204=
XM_011524438.1:c.612A>G (NAGS)	XP_011522740.1:p.Val204=
XM_011524439.1:c.114A>G (NAGS)	XP_011522741.1:p.Val38=
XM_011525035.1:c.-463+17750T>C (PYY)	XP_011523337.1:n.-463+17750T>C
XM_011524439.2:c.114A>G (NAGS)	XP_011522741.1:p.Val38=
NM_153006.3:c.612A>G (NAGS) MANE Select	NP_694551.1:p.Val204=