Canonical Allele Identifier: CA658824684
Gene: ARSA HGNC NCBI

Linked Data

ClinVar Variation Id: 552604
ClinVar RCV Id: RCV000667899
dbSNP Id: rs1555900463
MyVariant Identifiers: chr22:g.50626007del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50626008del , CM000684.2:g.50626008del GRCh38
NC_000022.10:g.51064436del , CM000684.1:g.51064436del GRCh37
NC_000022.9:g.49411302del NCBI36
NG_009260.2:g.7173del

Transcript Alleles

HGVS Amino-acid change
ENST00000216124.10:c.1036del MANE Select ENSP00000216124.5:p.Ala346LeufsTer?
ENST00000216124.9:c.1036del ENSP00000216124.5:p.Ala346LeufsTer?
ENST00000356098.9:c.1036del ENSP00000348406.5:p.Ala346LeufsTer?
ENST00000395619.3:c.1036del ENSP00000378981.3:p.Ala346LeufsTer?
ENST00000395621.7:c.1036del ENSP00000378983.3:p.Ala346LeufsTer?
ENST00000453344.6:c.778del ENSP00000412542.2:p.Ala260LeufsTer?
NM_000487.5:c.1036del NP_000478.3:p.Ala346LeufsTer?
NM_001085425.2:c.1036del NP_001078894.2:p.Ala346LeufsTer?
NM_001085426.2:c.1036del NP_001078895.2:p.Ala346LeufsTer?
NM_001085427.2:c.1036del NP_001078896.2:p.Ala346LeufsTer?
NM_001085428.2:c.778del NP_001078897.1:p.Ala260LeufsTer?
XM_011530690.1:c.778del XP_011528992.1:p.Ala260LeufsTer?
XM_011530691.1:c.1036del XP_011528993.1:p.Ala346LeufsTer29
NM_001362782.1:c.778del NP_001349711.1:p.Ala260LeufsTer?
XM_011530691.3:c.1036del XP_011528993.1:p.Ala346LeufsTer29
XM_017028800.1:c.1036del XP_016884289.1:p.Ala346LeufsTer?
XM_024452241.1:c.1036del XP_024308009.1:p.Ala346LeufsTer29
NM_000487.6:c.1036del MANE Select NP_000478.3:p.Ala346LeufsTer?
NM_001085425.3:c.1036del NP_001078894.2:p.Ala346LeufsTer?
NM_001085426.3:c.1036del NP_001078895.2:p.Ala346LeufsTer?
NM_001085427.3:c.1036del NP_001078896.2:p.Ala346LeufsTer?
NM_001085428.3:c.778del NP_001078897.1:p.Ala260LeufsTer?
NM_001362782.2:c.778del NP_001349711.1:p.Ala260LeufsTer?