Canonical Allele Identifier: CA2580099982
Gene: ARSA HGNC NCBI

Linked Data

ClinVar Variation Id: 2101566
ClinVar RCV Id: RCV003037475

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50627036_50627056del , CM000684.2:g.50627036_50627056del GRCh38
NC_000022.10:g.51065464_51065484del , CM000684.1:g.51065464_51065484del GRCh37
NC_000022.9:g.49412330_49412350del NCBI36
NG_009260.2:g.6124_6144del

Transcript Alleles

HGVS Amino-acid change
ENST00000216124.10:c.466-4_482del
ENST00000216124.9:c.466-4_482del
ENST00000356098.9:c.466-4_482del
ENST00000395619.3:c.466-4_482del
ENST00000395621.7:c.466-4_482del
ENST00000453344.6:c.208-4_224del
ENST00000551731.1:n.966_986del
NM_000487.5:c.466-4_482del
NM_001085425.2:c.466-4_482del
NM_001085426.2:c.466-4_482del
NM_001085427.2:c.466-4_482del
NM_001085428.2:c.208-4_224del
XM_011530690.1:c.208-4_224del
XM_011530691.1:c.466-4_482del
NM_001362782.1:c.208-4_224del
XM_011530691.3:c.466-4_482del
XM_017028800.1:c.466-4_482del
XM_024452241.1:c.466-4_482del
NM_000487.6:c.466-4_482del
NM_001085425.3:c.466-4_482del
NM_001085426.3:c.466-4_482del
NM_001085427.3:c.466-4_482del
NM_001085428.3:c.208-4_224del
NM_001362782.2:c.208-4_224del