Canonical Allele Identifier: CA626102852

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs1344734291
• gnomAD v2: 17-42085151-G-T
• gnomAD v4: 17-44007783-G-T
• MyVariant Identifiers: chr17:g.42085151G>T (hg19) ; chr17:g.44007783G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007783G>T , CM000679.2:g.44007783G>T	GRCh38
NC_000017.10:g.42085151G>T , CM000679.1:g.42085151G>T	GRCh37
NC_000017.9:g.39440677G>T	NCBI36
NG_008106.1:g.8120G>T
NG_023338.1:g.1687C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1451+10G>T (NAGS) MANE Select	ENSP00000293404.2:n.1451+10G>T
ENST00000293404.7:c.1451+10G>T (NAGS)	ENSP00000293404.2:n.1451+10G>T
ENST00000589767.1:c.1382+10G>T (NAGS)	ENSP00000465408.1:n.1382+10G>T
ENST00000592915.1:n.1339+10G>T (NAGS)
NM_153006.2:c.1451+10G>T (NAGS)	NP_694551.1:n.1451+10G>T
XM_011524438.1:c.1268+289G>T (NAGS)	XP_011522740.1:n.1268+289G>T
XM_011524439.1:c.953+10G>T (NAGS)	XP_011522741.1:n.953+10G>T
XM_011525035.1:c.-463+15789C>A (PYY)	XP_011523337.1:n.-463+15789C>A
XM_011524439.2:c.953+10G>T (NAGS)	XP_011522741.1:n.953+10G>T
NM_153006.3:c.1451+10G>T (NAGS) MANE Select	NP_694551.1:n.1451+10G>T