Canonical Allele Identifier: CA8595307

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs769606435
• ExAC: 17:42084101 G / T
• gnomAD v4: 17-44006733-G-T
• MyVariant Identifiers: chr17:g.42084101G>T (hg19) ; chr17:g.44006733G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006733G>T , CM000679.2:g.44006733G>T	GRCh38
NC_000017.10:g.42084101G>T , CM000679.1:g.42084101G>T	GRCh37
NC_000017.9:g.39439627G>T	NCBI36
NG_008106.1:g.7070G>T
NG_023338.1:g.2737C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1096+24G>T (NAGS) MANE Select	ENSP00000293404.2:n.1096+24G>T
ENST00000293404.7:c.1096+24G>T (NAGS)	ENSP00000293404.2:n.1096+24G>T
ENST00000589767.1:c.1003+24G>T (NAGS)	ENSP00000465408.1:n.1003+24G>T
ENST00000592915.1:n.395G>T (NAGS)
NM_153006.2:c.1096+24G>T (NAGS)	NP_694551.1:n.1096+24G>T
XM_011524438.1:c.1096+24G>T (NAGS)	XP_011522740.1:n.1096+24G>T
XM_011524439.1:c.598+24G>T (NAGS)	XP_011522741.1:n.598+24G>T
XM_011525035.1:c.-463+16839C>A (PYY)	XP_011523337.1:n.-463+16839C>A
XM_011524439.2:c.598+24G>T (NAGS)	XP_011522741.1:n.598+24G>T
NM_153006.3:c.1096+24G>T (NAGS) MANE Select	NP_694551.1:n.1096+24G>T