Canonical Allele Identifier: CA10645787

Gene: ARSA

Linked Data

• ClinVar Variation Id: 342199
• ClinVar RCV Id: RCV000407062
• dbSNP Id: rs8142531
• gnomAD v3: 22-50623669-C-T
• gnomAD v4: 22-50623669-C-T
• MyVariant Identifiers: chr22:g.51062097C>T (hg19) ; chr22:g.50623669C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50623669C>T , CM000684.2:g.50623669C>T	GRCh38
NC_000022.10:g.51062097C>T , CM000684.1:g.51062097C>T	GRCh37
NC_000022.9:g.49408963C>T	NCBI36
NG_009260.2:g.9511G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216124.10:c.*1476G>A MANE Select	ENSP00000216124.5:n.*1476G>A
ENST00000608497.1:c.302+105G>A
NM_000487.5:c.*1476G>A	NP_000478.3:n.*1476G>A
NM_001085425.2:c.*1476G>A	NP_001078894.2:n.*1476G>A
NM_001085426.2:c.*1476G>A	NP_001078895.2:n.*1476G>A
NM_001085427.2:c.*1476G>A	NP_001078896.2:n.*1476G>A
NM_001085428.2:c.*1476G>A	NP_001078897.1:n.*1476G>A
NM_001362782.1:c.*1476G>A	NP_001349711.1:n.*1476G>A
NM_000487.6:c.*1476G>A MANE Select	NP_000478.3:n.*1476G>A
NM_001085425.3:c.*1476G>A	NP_001078894.2:n.*1476G>A
NM_001085426.3:c.*1476G>A	NP_001078895.2:n.*1476G>A
NM_001085427.3:c.*1476G>A	NP_001078896.2:n.*1476G>A
NM_001085428.3:c.*1476G>A	NP_001078897.1:n.*1476G>A
NM_001362782.2:c.*1476G>A	NP_001349711.1:n.*1476G>A