Canonical Allele Identifier: CA290853814

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs1055474084
• MyVariant Identifiers: chr17:g.42084891T>A (hg19) ; chr17:g.44007523T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007523T>A , CM000679.2:g.44007523T>A	GRCh38
NC_000017.10:g.42084891T>A , CM000679.1:g.42084891T>A	GRCh37
NC_000017.9:g.39440417T>A	NCBI36
NG_008106.1:g.7860T>A
NG_023338.1:g.1947A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000293404.8:c.1268+29T>A (NAGS) MANE Select	ENSP00000293404.2:n.1268+29T>A
ENST00000293404.7:c.1268+29T>A (NAGS)	ENSP00000293404.2:n.1268+29T>A
ENST00000589767.1:c.1175+29T>A (NAGS)	ENSP00000465408.1:n.1175+29T>A
ENST00000592915.1:n.1156+29T>A (NAGS)
NM_153006.2:c.1268+29T>A (NAGS)	NP_694551.1:n.1268+29T>A
XM_011524438.1:c.1268+29T>A (NAGS)	XP_011522740.1:n.1268+29T>A
XM_011524439.1:c.770+29T>A (NAGS)	XP_011522741.1:n.770+29T>A
XM_011525035.1:c.-463+16049A>T (PYY)	XP_011523337.1:n.-463+16049A>T
XM_011524439.2:c.770+29T>A (NAGS)	XP_011522741.1:n.770+29T>A
NM_153006.3:c.1268+29T>A (NAGS) MANE Select	NP_694551.1:n.1268+29T>A