Canonical Allele Identifier: CA2580099970

Gene: ARSA

Linked Data

• ClinVar Variation Id: 1725391
• ClinVar RCV Id: RCV002309075

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50626909_50626910del , CM000684.2:g.50626909_50626910del	GRCh38
NC_000022.10:g.51065337_51065338del , CM000684.1:g.51065337_51065338del	GRCh37
NC_000022.9:g.49412203_49412204del	NCBI36
NG_009260.2:g.6271_6272del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216124.10:c.609_610del MANE Select	ENSP00000216124.5:p.Met204GlyfsTer5
ENST00000216124.9:c.609_610del	ENSP00000216124.5:p.Met204GlyfsTer5
ENST00000356098.9:c.609_610del	ENSP00000348406.5:p.Met204GlyfsTer5
ENST00000395619.3:c.609_610del	ENSP00000378981.3:p.Met204GlyfsTer5
ENST00000395621.7:c.609_610del	ENSP00000378983.3:p.Met204GlyfsTer5
ENST00000453344.6:c.351_352del	ENSP00000412542.2:p.Met118GlyfsTer5
ENST00000551731.1:n.1113_1114del
NM_000487.5:c.609_610del	NP_000478.3:p.Met204GlyfsTer5
NM_001085425.2:c.609_610del	NP_001078894.2:p.Met204GlyfsTer5
NM_001085426.2:c.609_610del	NP_001078895.2:p.Met204GlyfsTer5
NM_001085427.2:c.609_610del	NP_001078896.2:p.Met204GlyfsTer5
NM_001085428.2:c.351_352del	NP_001078897.1:p.Met118GlyfsTer5
XM_011530690.1:c.351_352del	XP_011528992.1:p.Met118GlyfsTer5
XM_011530691.1:c.609_610del	XP_011528993.1:p.Met204GlyfsTer5
NM_001362782.1:c.351_352del	NP_001349711.1:p.Met118GlyfsTer5
XM_011530691.3:c.609_610del	XP_011528993.1:p.Met204GlyfsTer5
XM_017028800.1:c.609_610del	XP_016884289.1:p.Met204GlyfsTer5
XM_024452241.1:c.609_610del	XP_024308009.1:p.Met204GlyfsTer5
NM_000487.6:c.609_610del MANE Select	NP_000478.3:p.Met204GlyfsTer5
NM_001085425.3:c.609_610del	NP_001078894.2:p.Met204GlyfsTer5
NM_001085426.3:c.609_610del	NP_001078895.2:p.Met204GlyfsTer5
NM_001085427.3:c.609_610del	NP_001078896.2:p.Met204GlyfsTer5
NM_001085428.3:c.351_352del	NP_001078897.1:p.Met118GlyfsTer5
NM_001362782.2:c.351_352del	NP_001349711.1:p.Met118GlyfsTer5