Canonical Allele Identifier: CA1026679336

Gene: ARSA

Linked Data

• dbSNP Id: rs2082633604
• gnomAD v3: 22-50624667-G-C
• gnomAD v4: 22-50624667-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50624667G>C , CM000684.2:g.50624667G>C	GRCh38
NC_000022.10:g.51063095G>C , CM000684.1:g.51063095G>C	GRCh37
NC_000022.9:g.49409961G>C	NCBI36
NG_009260.2:g.8513C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216124.10:c.*478C>G MANE Select	ENSP00000216124.5:n.*478C>G
ENST00000608497.1:c.180+696C>G
NM_000487.5:c.*478C>G	NP_000478.3:n.*478C>G
NM_001085425.2:c.*478C>G	NP_001078894.2:n.*478C>G
NM_001085426.2:c.*478C>G	NP_001078895.2:n.*478C>G
NM_001085427.2:c.*478C>G	NP_001078896.2:n.*478C>G
NM_001085428.2:c.*478C>G	NP_001078897.1:n.*478C>G
NM_001362782.1:c.*478C>G	NP_001349711.1:n.*478C>G
NM_000487.6:c.*478C>G MANE Select	NP_000478.3:n.*478C>G
NM_001085425.3:c.*478C>G	NP_001078894.2:n.*478C>G
NM_001085426.3:c.*478C>G	NP_001078895.2:n.*478C>G
NM_001085427.3:c.*478C>G	NP_001078896.2:n.*478C>G
NM_001085428.3:c.*478C>G	NP_001078897.1:n.*478C>G
NM_001362782.2:c.*478C>G	NP_001349711.1:n.*478C>G