Canonical Allele Identifier: CA500616081

Gene: NAGS PYY

Linked Data

• ClinVar Variation Id: 2968212
• ClinVar RCV Id: RCV003821338
• dbSNP Id: rs761562315
• gnomAD v3: 17-44006123-C-T
• gnomAD v4: 17-44006123-C-T
• MyVariant Identifiers: chr17:g.42083491C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006123C>T , CM000679.2:g.44006123C>T	GRCh38
NC_000017.10:g.42083491C>T , CM000679.1:g.42083491C>T	GRCh37
NC_000017.9:g.39439017C>T	NCBI36
NG_008106.1:g.6460C>T
NG_023338.1:g.3347G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.801C>T (NAGS) MANE Select	ENSP00000293404.2:p.Arg267=
ENST00000293404.7:c.801C>T (NAGS)	ENSP00000293404.2:p.Arg267=
ENST00000589767.1:c.708C>T (NAGS)	ENSP00000465408.1:p.Arg236=
ENST00000592915.1:n.76C>T (NAGS)
NM_153006.2:c.801C>T (NAGS)	NP_694551.1:p.Arg267=
XM_011524438.1:c.801C>T (NAGS)	XP_011522740.1:p.Arg267=
XM_011524439.1:c.303C>T (NAGS)	XP_011522741.1:p.Arg101=
XM_011525035.1:c.-463+17449G>A (PYY)	XP_011523337.1:n.-463+17449G>A
XM_011524439.2:c.303C>T (NAGS)	XP_011522741.1:p.Arg101=
NM_153006.3:c.801C>T (NAGS) MANE Select	NP_694551.1:p.Arg267=