Canonical Allele Identifier: CA626222685

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs1456568575
• gnomAD v2: 17-42084103-C-T
• gnomAD v4: 17-44006735-C-T
• MyVariant Identifiers: chr17:g.42084103C>T (hg19) ; chr17:g.44006735C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006735C>T , CM000679.2:g.44006735C>T	GRCh38
NC_000017.10:g.42084103C>T , CM000679.1:g.42084103C>T	GRCh37
NC_000017.9:g.39439629C>T	NCBI36
NG_008106.1:g.7072C>T
NG_023338.1:g.2735G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1096+26C>T (NAGS) MANE Select	ENSP00000293404.2:n.1096+26C>T
ENST00000293404.7:c.1096+26C>T (NAGS)	ENSP00000293404.2:n.1096+26C>T
ENST00000589767.1:c.1003+26C>T (NAGS)	ENSP00000465408.1:n.1003+26C>T
ENST00000592915.1:n.397C>T (NAGS)
NM_153006.2:c.1096+26C>T (NAGS)	NP_694551.1:n.1096+26C>T
XM_011524438.1:c.1096+26C>T (NAGS)	XP_011522740.1:n.1096+26C>T
XM_011524439.1:c.598+26C>T (NAGS)	XP_011522741.1:n.598+26C>T
XM_011525035.1:c.-463+16837G>A (PYY)	XP_011523337.1:n.-463+16837G>A
XM_011524439.2:c.598+26C>T (NAGS)	XP_011522741.1:n.598+26C>T
NM_153006.3:c.1096+26C>T (NAGS) MANE Select	NP_694551.1:n.1096+26C>T