Canonical Allele Identifier: CA916084121
Gene: ARSA HGNC NCBI

Linked Data

ClinVar Variation Id: 856376
ClinVar RCV Id: RCV001061823
dbSNP Id: rs2082684340

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50627053del , CM000684.2:g.50627053del GRCh38
NC_000022.10:g.51065481del , CM000684.1:g.51065481del GRCh37
NC_000022.9:g.49412347del NCBI36
NG_009260.2:g.6129del

Transcript Alleles

HGVS Amino-acid change
ENST00000216124.10:c.467del
ENST00000216124.9:c.467del
ENST00000356098.9:c.467del
ENST00000395619.3:c.467del
ENST00000395621.7:c.467del
ENST00000453344.6:c.209del
ENST00000551731.1:n.971del
NM_000487.5:c.467del
NM_001085425.2:c.467del
NM_001085426.2:c.467del
NM_001085427.2:c.467del
NM_001085428.2:c.209del
XM_011530690.1:c.209del
XM_011530691.1:c.467del
NM_001362782.1:c.209del
XM_011530691.3:c.467del
XM_017028800.1:c.467del
XM_024452241.1:c.467del
NM_000487.6:c.467del
NM_001085425.3:c.467del
NM_001085426.3:c.467del
NM_001085427.3:c.467del
NM_001085428.3:c.209del
NM_001362782.2:c.209del