Canonical Allele Identifier: CA2576286566

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006716del , CM000679.2:g.44006716del GRCh38
NC_000017.10:g.42084084del , CM000679.1:g.42084084del GRCh37
NC_000017.9:g.39439610del NCBI36
NG_008106.1:g.7053del
NG_023338.1:g.2756del

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.1096+7del (NAGS) MANE Select ENSP00000293404.2:n.1096+7del
ENST00000293404.7:c.1096+7del (NAGS) ENSP00000293404.2:n.1096+7del
ENST00000589767.1:c.1003+7del (NAGS) ENSP00000465408.1:n.1003+7del
ENST00000592915.1:n.378del (NAGS)
NM_153006.2:c.1096+7del (NAGS) NP_694551.1:n.1096+7del
XM_011524438.1:c.1096+7del (NAGS) XP_011522740.1:n.1096+7del
XM_011524439.1:c.598+7del (NAGS) XP_011522741.1:n.598+7del
XM_011525035.1:c.-463+16858del (PYY) XP_011523337.1:n.-463+16858del
XM_011524439.2:c.598+7del (NAGS) XP_011522741.1:n.598+7del
NM_153006.3:c.1096+7del (NAGS) MANE Select NP_694551.1:n.1096+7del