Canonical Allele Identifier: CA399726109

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs1203280225
• gnomAD v2: 17-42083937-T-C
• gnomAD v4: 17-44006569-T-C
• COSMIC: COSM6377639
• MyVariant Identifiers: chr17:g.42083937T>C (hg19) ; chr17:g.44006569T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006569T>C , CM000679.2:g.44006569T>C	GRCh38
NC_000017.10:g.42083937T>C , CM000679.1:g.42083937T>C	GRCh37
NC_000017.9:g.39439463T>C	NCBI36
NG_008106.1:g.6906T>C
NG_023338.1:g.2901A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.956T>C (NAGS) MANE Select	ENSP00000293404.2:p.Val319Ala
ENST00000293404.7:c.956T>C (NAGS)	ENSP00000293404.2:p.Val319Ala
ENST00000589767.1:c.863T>C (NAGS)	ENSP00000465408.1:p.Val288Ala
ENST00000592915.1:n.231T>C (NAGS)
NM_153006.2:c.956T>C (NAGS)	NP_694551.1:p.Val319Ala
XM_011524438.1:c.956T>C (NAGS)	XP_011522740.1:p.Val319Ala
XM_011524439.1:c.458T>C (NAGS)	XP_011522741.1:p.Val153Ala
XM_011525035.1:c.-463+17003A>G (PYY)	XP_011523337.1:n.-463+17003A>G
XM_011524439.2:c.458T>C (NAGS)	XP_011522741.1:p.Val153Ala
NM_153006.3:c.956T>C (NAGS) MANE Select	NP_694551.1:p.Val319Ala