Canonical Allele Identifier: CA2839651685
Gene: ARSA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50627762dup , CM000684.2:g.50627762dup GRCh38
NC_000022.10:g.51066190dup , CM000684.1:g.51066190dup GRCh37
NC_000022.9:g.49413056dup NCBI36
NG_009260.2:g.5418dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000216124.10:c.18dup MANE Select ENSP00000216124.5:p.Arg7AlafsTer?
ENST00000216124.9:c.18dup ENSP00000216124.5:p.Arg7AlafsTer?
ENST00000356098.9:c.18dup ENSP00000348406.5:p.Arg7AlafsTer?
ENST00000395619.3:c.18dup ENSP00000378981.3:p.Arg7AlafsTer?
ENST00000395621.7:c.18dup ENSP00000378983.3:p.Arg7AlafsTer?
ENST00000453344.6:c.-35+184dup ENSP00000412542.2:n.-35+184dup
ENST00000551731.1:n.409dup
NM_000487.5:c.18dup NP_000478.3:p.Arg7AlafsTer?
NM_001085425.2:c.18dup NP_001078894.2:p.Arg7AlafsTer?
NM_001085426.2:c.18dup NP_001078895.2:p.Arg7AlafsTer?
NM_001085427.2:c.18dup NP_001078896.2:p.Arg7AlafsTer?
NM_001085428.2:c.-35+184dup NP_001078897.1:n.-35+184dup
XM_011530690.1:c.-35+229dup XP_011528992.1:n.-35+229dup
XM_011530691.1:c.18dup XP_011528993.1:p.Arg7AlafsTer?
NM_001362782.1:c.-35+229dup NP_001349711.1:n.-35+229dup
XM_011530691.3:c.18dup XP_011528993.1:p.Arg7AlafsTer?
XM_017028800.1:c.18dup XP_016884289.1:p.Arg7AlafsTer?
XM_024452241.1:c.18dup XP_024308009.1:p.Arg7AlafsTer?
NM_000487.6:c.18dup MANE Select NP_000478.3:p.Arg7AlafsTer?
NM_001085425.3:c.18dup NP_001078894.2:p.Arg7AlafsTer?
NM_001085426.3:c.18dup NP_001078895.2:p.Arg7AlafsTer?
NM_001085427.3:c.18dup NP_001078896.2:p.Arg7AlafsTer?
NM_001085428.3:c.-35+184dup NP_001078897.1:n.-35+184dup
NM_001362782.2:c.-35+229dup NP_001349711.1:n.-35+229dup