Canonical Allele Identifier: CA2261182137

Gene: NAGS PYY

Linked Data

• dbSNP Id: rs1186034913
• gnomAD v4: 17-44006473-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006479del , CM000679.2:g.44006479del	GRCh38
NC_000017.10:g.42083847del , CM000679.1:g.42083847del	GRCh37
NC_000017.9:g.39439373del	NCBI36
NG_008106.1:g.6816del
NG_023338.1:g.2996del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.916-50del (NAGS) MANE Select	ENSP00000293404.2:n.916-50del
ENST00000293404.7:c.916-50del (NAGS)	ENSP00000293404.2:n.916-50del
ENST00000589767.1:c.823-50del (NAGS)	ENSP00000465408.1:n.823-50del
ENST00000592915.1:n.191-50del (NAGS)
NM_153006.2:c.916-50del (NAGS)	NP_694551.1:n.916-50del
XM_011524438.1:c.916-50del (NAGS)	XP_011522740.1:n.916-50del
XM_011524439.1:c.418-50del (NAGS)	XP_011522741.1:n.418-50del
XM_011525035.1:c.-463+17098del (PYY)	XP_011523337.1:n.-463+17098del
XM_011524439.2:c.418-50del (NAGS)	XP_011522741.1:n.418-50del
NM_153006.3:c.916-50del (NAGS) MANE Select	NP_694551.1:n.916-50del