Canonical Allele Identifier: CA754066859

Gene: ARSA

Linked Data

• ClinVar Variation Id: 903296
• ClinVar RCV Id: RCV001150509
• dbSNP Id: rs1181265537
• gnomAD v3: 22-50624679-G-A
• gnomAD v4: 22-50624679-G-A
• MyVariant Identifiers: chr22:g.51063107G>A (hg19) ; chr22:g.50624679G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50624679G>A , CM000684.2:g.50624679G>A	GRCh38
NC_000022.10:g.51063107G>A , CM000684.1:g.51063107G>A	GRCh37
NC_000022.9:g.49409973G>A	NCBI36
NG_009260.2:g.8501C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216124.10:c.*466C>T MANE Select	ENSP00000216124.5:n.*466C>T
ENST00000608497.1:c.180+684C>T
NM_000487.5:c.*466C>T	NP_000478.3:n.*466C>T
NM_001085425.2:c.*466C>T	NP_001078894.2:n.*466C>T
NM_001085426.2:c.*466C>T	NP_001078895.2:n.*466C>T
NM_001085427.2:c.*466C>T	NP_001078896.2:n.*466C>T
NM_001085428.2:c.*466C>T	NP_001078897.1:n.*466C>T
NM_001362782.1:c.*466C>T	NP_001349711.1:n.*466C>T
NM_000487.6:c.*466C>T MANE Select	NP_000478.3:n.*466C>T
NM_001085425.3:c.*466C>T	NP_001078894.2:n.*466C>T
NM_001085426.3:c.*466C>T	NP_001078895.2:n.*466C>T
NM_001085427.3:c.*466C>T	NP_001078896.2:n.*466C>T
NM_001085428.3:c.*466C>T	NP_001078897.1:n.*466C>T
NM_001362782.2:c.*466C>T	NP_001349711.1:n.*466C>T