Canonical Allele Identifier: CA2638146954

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007680del , CM000679.2:g.44007680del GRCh38
NC_000017.10:g.42085048del , CM000679.1:g.42085048del GRCh37
NC_000017.9:g.39440574del NCBI36
NG_008106.1:g.8017del
NG_023338.1:g.1792del

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1358del (NAGS) MANE Select ENSP00000293404.2:p.Gly453AlafsTer?
ENST00000293404.7:c.1358del (NAGS) ENSP00000293404.2:p.Gly453AlafsTer?
ENST00000589767.1:c.1289del (NAGS) ENSP00000465408.1:p.Gly430AlafsTer?
ENST00000592915.1:n.1246del (NAGS)
NM_153006.2:c.1358del (NAGS) NP_694551.1:p.Gly453AlafsTer?
XM_011524438.1:c.1268+186del (NAGS) XP_011522740.1:n.1268+186del
XM_011524439.1:c.860del (NAGS) XP_011522741.1:p.Gly287AlafsTer?
XM_011525035.1:c.-463+15894del (PYY) XP_011523337.1:n.-463+15894del
XM_011524439.2:c.860del (NAGS) XP_011522741.1:p.Gly287AlafsTer?
NM_153006.3:c.1358del (NAGS) MANE Select NP_694551.1:p.Gly453AlafsTer?