Canonical Allele Identifier: CA412177333
Gene: ARSA HGNC NCBI

Linked Data

ClinVar Variation Id: 996131
ClinVar RCV Id: RCV001290420
dbSNP Id: rs2082680103

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50626911A>G , CM000684.2:g.50626911A>G GRCh38
NC_000022.10:g.51065339A>G , CM000684.1:g.51065339A>G GRCh37
NC_000022.9:g.49412205A>G NCBI36
NG_009260.2:g.6269T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216124.10:c.607T>C MANE Select ENSP00000216124.5:p.Tyr203His
ENST00000216124.9:c.607T>C ENSP00000216124.5:p.Tyr203His
ENST00000356098.9:c.607T>C ENSP00000348406.5:p.Tyr203His
ENST00000395619.3:c.607T>C ENSP00000378981.3:p.Tyr203His
ENST00000395621.7:c.607T>C ENSP00000378983.3:p.Tyr203His
ENST00000453344.6:c.349T>C ENSP00000412542.2:p.Tyr117His
ENST00000551731.1:n.1111T>C
NM_000487.5:c.607T>C NP_000478.3:p.Tyr203His
NM_001085425.2:c.607T>C NP_001078894.2:p.Tyr203His
NM_001085426.2:c.607T>C NP_001078895.2:p.Tyr203His
NM_001085427.2:c.607T>C NP_001078896.2:p.Tyr203His
NM_001085428.2:c.349T>C NP_001078897.1:p.Tyr117His
XM_011530690.1:c.349T>C XP_011528992.1:p.Tyr117His
XM_011530691.1:c.607T>C XP_011528993.1:p.Tyr203His
NM_001362782.1:c.349T>C NP_001349711.1:p.Tyr117His
XM_011530691.3:c.607T>C XP_011528993.1:p.Tyr203His
XM_017028800.1:c.607T>C XP_016884289.1:p.Tyr203His
XM_024452241.1:c.607T>C XP_024308009.1:p.Tyr203His
NM_000487.6:c.607T>C MANE Select NP_000478.3:p.Tyr203His
NM_001085425.3:c.607T>C NP_001078894.2:p.Tyr203His
NM_001085426.3:c.607T>C NP_001078895.2:p.Tyr203His
NM_001085427.3:c.607T>C NP_001078896.2:p.Tyr203His
NM_001085428.3:c.349T>C NP_001078897.1:p.Tyr117His
NM_001362782.2:c.349T>C NP_001349711.1:p.Tyr117His