Canonical Allele Identifier: CA278422
Gene: ARSA HGNC NCBI

Linked Data

ClinVar Variation Id: 93121
dbSNP Id: rs398123414

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50627585del , CM000684.2:g.50627585del GRCh38
NC_000022.10:g.51066013del , CM000684.1:g.51066013del GRCh37
NC_000022.9:g.49412879del NCBI36
NG_009260.2:g.5595del

Transcript Alleles

HGVS Amino-acid change
ENST00000216124.10:c.195del MANE Select ENSP00000216124.5:p.Tyr65Ter
ENST00000216124.9:c.195del ENSP00000216124.5:p.Tyr65Ter
ENST00000356098.9:c.195del ENSP00000348406.5:p.Tyr65Ter
ENST00000395619.3:c.195del ENSP00000378981.3:p.Tyr65Ter
ENST00000395621.7:c.195del ENSP00000378983.3:p.Tyr65Ter
ENST00000453344.6:c.-34-179del ENSP00000412542.2:n.-34-179del
ENST00000551731.1:n.586del
NM_000487.5:c.195del NP_000478.3:p.Tyr65Ter
NM_001085425.2:c.195del NP_001078894.2:p.Tyr65Ter
NM_001085426.2:c.195del NP_001078895.2:p.Tyr65Ter
NM_001085427.2:c.195del NP_001078896.2:p.Tyr65Ter
NM_001085428.2:c.-34-179del NP_001078897.1:n.-34-179del
XM_011530690.1:c.-34-179del XP_011528992.1:n.-34-179del
XM_011530691.1:c.195del XP_011528993.1:p.Tyr65Ter
NM_001362782.1:c.-34-179del NP_001349711.1:n.-34-179del
XM_011530691.3:c.195del XP_011528993.1:p.Tyr65Ter
XM_017028800.1:c.195del XP_016884289.1:p.Tyr65Ter
XM_024452241.1:c.195del XP_024308009.1:p.Tyr65Ter
NM_000487.6:c.195del MANE Select NP_000478.3:p.Tyr65Ter
NM_001085425.3:c.195del NP_001078894.2:p.Tyr65Ter
NM_001085426.3:c.195del NP_001078895.2:p.Tyr65Ter
NM_001085427.3:c.195del NP_001078896.2:p.Tyr65Ter
NM_001085428.3:c.-34-179del NP_001078897.1:n.-34-179del
NM_001362782.2:c.-34-179del NP_001349711.1:n.-34-179del