Canonical Allele Identifier: CA913088709
Gene: ARSA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50627221_50627233del , CM000684.2:g.50627221_50627233del GRCh38
NC_000022.10:g.51065649_51065661del , CM000684.1:g.51065649_51065661del GRCh37
NC_000022.9:g.49412515_49412527del NCBI36
NG_009260.2:g.5947_5959del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216124.10:c.398_410del MANE Select ENSP00000216124.5:p.Glu133GlyfsTer11
ENST00000216124.9:c.398_410del ENSP00000216124.5:p.Glu133GlyfsTer11
ENST00000356098.9:c.398_410del ENSP00000348406.5:p.Glu133GlyfsTer11
ENST00000395619.3:c.398_410del ENSP00000378981.3:p.Glu133GlyfsTer11
ENST00000395621.7:c.398_410del ENSP00000378983.3:p.Glu133GlyfsTer11
ENST00000453344.6:c.140_152del ENSP00000412542.2:p.Glu47GlyfsTer11
ENST00000551731.1:n.789_801del
NM_000487.5:c.398_410del NP_000478.3:p.Glu133GlyfsTer11
NM_001085425.2:c.398_410del NP_001078894.2:p.Glu133GlyfsTer11
NM_001085426.2:c.398_410del NP_001078895.2:p.Glu133GlyfsTer11
NM_001085427.2:c.398_410del NP_001078896.2:p.Glu133GlyfsTer11
NM_001085428.2:c.140_152del NP_001078897.1:p.Glu47GlyfsTer11
XM_011530690.1:c.140_152del XP_011528992.1:p.Glu47GlyfsTer11
XM_011530691.1:c.398_410del XP_011528993.1:p.Glu133GlyfsTer11
NM_001362782.1:c.140_152del NP_001349711.1:p.Glu47GlyfsTer11
XM_011530691.3:c.398_410del XP_011528993.1:p.Glu133GlyfsTer11
XM_017028800.1:c.398_410del XP_016884289.1:p.Glu133GlyfsTer11
XM_024452241.1:c.398_410del XP_024308009.1:p.Glu133GlyfsTer11
NM_000487.6:c.398_410del MANE Select NP_000478.3:p.Glu133GlyfsTer11
NM_001085425.3:c.398_410del NP_001078894.2:p.Glu133GlyfsTer11
NM_001085426.3:c.398_410del NP_001078895.2:p.Glu133GlyfsTer11
NM_001085427.3:c.398_410del NP_001078896.2:p.Glu133GlyfsTer11
NM_001085428.3:c.140_152del NP_001078897.1:p.Glu47GlyfsTer11
NM_001362782.2:c.140_152del NP_001349711.1:p.Glu47GlyfsTer11