Canonical Allele Identifier: CA2638147001

Gene: NAGS PYY

Linked Data

• gnomAD v4: 17-44007811-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007811A>T , CM000679.2:g.44007811A>T	GRCh38
NC_000017.10:g.42085179A>T , CM000679.1:g.42085179A>T	GRCh37
NC_000017.9:g.39440705A>T	NCBI36
NG_008106.1:g.8148A>T
NG_023338.1:g.1659T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1451+38A>T (NAGS) MANE Select	ENSP00000293404.2:n.1451+38A>T
ENST00000293404.7:c.1451+38A>T (NAGS)	ENSP00000293404.2:n.1451+38A>T
ENST00000589767.1:c.1382+38A>T (NAGS)	ENSP00000465408.1:n.1382+38A>T
ENST00000592915.1:n.1339+38A>T (NAGS)
NM_153006.2:c.1451+38A>T (NAGS)	NP_694551.1:n.1451+38A>T
XM_011524438.1:c.1268+317A>T (NAGS)	XP_011522740.1:n.1268+317A>T
XM_011524439.1:c.953+38A>T (NAGS)	XP_011522741.1:n.953+38A>T
XM_011525035.1:c.-463+15761T>A (PYY)	XP_011523337.1:n.-463+15761T>A
XM_011524439.2:c.953+38A>T (NAGS)	XP_011522741.1:n.953+38A>T
NM_153006.3:c.1451+38A>T (NAGS) MANE Select	NP_694551.1:n.1451+38A>T