Canonical Allele Identifier: CA399726233

Gene: NAGS PYY

Linked Data

• MyVariant Identifiers: chr17:g.42083968A>T (hg19) ; chr17:g.44006600A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006600A>T , CM000679.2:g.44006600A>T	GRCh38
NC_000017.10:g.42083968A>T , CM000679.1:g.42083968A>T	GRCh37
NC_000017.9:g.39439494A>T	NCBI36
NG_008106.1:g.6937A>T
NG_023338.1:g.2870T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.987A>T (NAGS) MANE Select	ENSP00000293404.2:p.Glu329Asp
ENST00000293404.7:c.987A>T (NAGS)	ENSP00000293404.2:p.Glu329Asp
ENST00000589767.1:c.894A>T (NAGS)	ENSP00000465408.1:p.Glu298Asp
ENST00000592915.1:n.262A>T (NAGS)
NM_153006.2:c.987A>T (NAGS)	NP_694551.1:p.Glu329Asp
XM_011524438.1:c.987A>T (NAGS)	XP_011522740.1:p.Glu329Asp
XM_011524439.1:c.489A>T (NAGS)	XP_011522741.1:p.Glu163Asp
XM_011525035.1:c.-463+16972T>A (PYY)	XP_011523337.1:n.-463+16972T>A
XM_011524439.2:c.489A>T (NAGS)	XP_011522741.1:p.Glu163Asp
NM_153006.3:c.987A>T (NAGS) MANE Select	NP_694551.1:p.Glu329Asp