Canonical Allele Identifier: CA2695200250

Linked Data

ClinVar Variation Id: 2676907
ClinVar RCV Id: RCV003463080

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006164del , CM000679.2:g.44006164del GRCh38
NC_000017.10:g.42083532del , CM000679.1:g.42083532del GRCh37
NC_000017.9:g.39439058del NCBI36
NG_008106.1:g.6501del
NG_023338.1:g.3306del

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.842del (NAGS) MANE Select ENSP00000293404.2:p.Leu281ArgfsTer27
ENST00000293404.7:c.842del (NAGS) ENSP00000293404.2:p.Leu281ArgfsTer27
ENST00000589767.1:c.749del (NAGS) ENSP00000465408.1:p.Leu250ArgfsTer27
ENST00000592915.1:n.117del (NAGS)
NM_153006.2:c.842del (NAGS) NP_694551.1:p.Leu281ArgfsTer27
XM_011524438.1:c.842del (NAGS) XP_011522740.1:p.Leu281ArgfsTer27
XM_011524439.1:c.344del (NAGS) XP_011522741.1:p.Leu115ArgfsTer27
XM_011525035.1:c.-463+17408del (PYY) XP_011523337.1:n.-463+17408del
XM_011524439.2:c.344del (NAGS) XP_011522741.1:p.Leu115ArgfsTer27
NM_153006.3:c.842del (NAGS) MANE Select NP_694551.1:p.Leu281ArgfsTer27