Canonical Allele Identifier: CA2638146939

Gene: NAGS PYY

Linked Data

• gnomAD v4: 17-44007534-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44007534G>A , CM000679.2:g.44007534G>A	GRCh38
NC_000017.10:g.42084902G>A , CM000679.1:g.42084902G>A	GRCh37
NC_000017.9:g.39440428G>A	NCBI36
NG_008106.1:g.7871G>A
NG_023338.1:g.1936C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000293404.8:c.1268+40G>A (NAGS) MANE Select	ENSP00000293404.2:n.1268+40G>A
ENST00000293404.7:c.1268+40G>A (NAGS)	ENSP00000293404.2:n.1268+40G>A
ENST00000589767.1:c.1176-33G>A (NAGS)	ENSP00000465408.1:n.1176-33G>A
ENST00000592915.1:n.1156+40G>A (NAGS)
NM_153006.2:c.1268+40G>A (NAGS)	NP_694551.1:n.1268+40G>A
XM_011524438.1:c.1268+40G>A (NAGS)	XP_011522740.1:n.1268+40G>A
XM_011524439.1:c.770+40G>A (NAGS)	XP_011522741.1:n.770+40G>A
XM_011525035.1:c.-463+16038C>T (PYY)	XP_011523337.1:n.-463+16038C>T
XM_011524439.2:c.770+40G>A (NAGS)	XP_011522741.1:n.770+40G>A
NM_153006.3:c.1268+40G>A (NAGS) MANE Select	NP_694551.1:n.1268+40G>A