Canonical Allele Identifier: CA2638145893

Gene: NAGS PYY

Linked Data

• gnomAD v4: 17-44006729-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44006733del , CM000679.2:g.44006733del	GRCh38
NC_000017.10:g.42084101del , CM000679.1:g.42084101del	GRCh37
NC_000017.9:g.39439627del	NCBI36
NG_008106.1:g.7070del
NG_023338.1:g.2740del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293404.8:c.1096+24del (NAGS) MANE Select	ENSP00000293404.2:n.1096+24del
ENST00000293404.7:c.1096+24del (NAGS)	ENSP00000293404.2:n.1096+24del
ENST00000589767.1:c.1003+24del (NAGS)	ENSP00000465408.1:n.1003+24del
ENST00000592915.1:n.395del (NAGS)
NM_153006.2:c.1096+24del (NAGS)	NP_694551.1:n.1096+24del
XM_011524438.1:c.1096+24del (NAGS)	XP_011522740.1:n.1096+24del
XM_011524439.1:c.598+24del (NAGS)	XP_011522741.1:n.598+24del
XM_011525035.1:c.-463+16842del (PYY)	XP_011523337.1:n.-463+16842del
XM_011524439.2:c.598+24del (NAGS)	XP_011522741.1:n.598+24del
NM_153006.3:c.1096+24del (NAGS) MANE Select	NP_694551.1:n.1096+24del