Canonical Allele Identifier: CA399726170

Gene: NAGS PYY

Linked Data

• gnomAD v4: 17-44006584-G-T
• MyVariant Identifiers: chr17:g.42083952G>T (hg19) ; chr17:g.44006584G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006584G>T , CM000679.2:g.44006584G>T	GRCh38
NC_000017.10:g.42083952G>T , CM000679.1:g.42083952G>T	GRCh37
NC_000017.9:g.39439478G>T	NCBI36
NG_008106.1:g.6921G>T
NG_023338.1:g.2886C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000293404.8:c.971G>T (NAGS) MANE Select	ENSP00000293404.2:p.Trp324Leu
ENST00000293404.7:c.971G>T (NAGS)	ENSP00000293404.2:p.Trp324Leu
ENST00000589767.1:c.878G>T (NAGS)	ENSP00000465408.1:p.Trp293Leu
ENST00000592915.1:n.246G>T (NAGS)
NM_153006.2:c.971G>T (NAGS)	NP_694551.1:p.Trp324Leu
XM_011524438.1:c.971G>T (NAGS)	XP_011522740.1:p.Trp324Leu
XM_011524439.1:c.473G>T (NAGS)	XP_011522741.1:p.Trp158Leu
XM_011525035.1:c.-463+16988C>A (PYY)	XP_011523337.1:n.-463+16988C>A
XM_011524439.2:c.473G>T (NAGS)	XP_011522741.1:p.Trp158Leu
NM_153006.3:c.971G>T (NAGS) MANE Select	NP_694551.1:p.Trp324Leu