Canonical Allele Identifier: CA640358664
Gene: ARSA HGNC NCBI

Linked Data

dbSNP Id: rs1223366135

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50626122C>T , CM000684.2:g.50626122C>T GRCh38
NC_000022.10:g.51064550C>T , CM000684.1:g.51064550C>T GRCh37
NC_000022.9:g.49411416C>T NCBI36
NG_009260.2:g.7058G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000216124.10:c.979+32G>A MANE Select ENSP00000216124.5:n.979+32G>A
ENST00000216124.9:c.979+32G>A ENSP00000216124.5:n.979+32G>A
ENST00000356098.9:c.979+32G>A ENSP00000348406.5:n.979+32G>A
ENST00000395619.3:c.979+32G>A ENSP00000378981.3:n.979+32G>A
ENST00000395621.7:c.979+32G>A ENSP00000378983.3:n.979+32G>A
ENST00000453344.6:c.721+32G>A ENSP00000412542.2:n.721+32G>A
NM_000487.5:c.979+32G>A NP_000478.3:n.979+32G>A
NM_001085425.2:c.979+32G>A NP_001078894.2:n.979+32G>A
NM_001085426.2:c.979+32G>A NP_001078895.2:n.979+32G>A
NM_001085427.2:c.979+32G>A NP_001078896.2:n.979+32G>A
NM_001085428.2:c.721+32G>A NP_001078897.1:n.721+32G>A
XM_011530690.1:c.721+32G>A XP_011528992.1:n.721+32G>A
XM_011530691.1:c.979+32G>A XP_011528993.1:n.979+32G>A
NM_001362782.1:c.721+32G>A NP_001349711.1:n.721+32G>A
XM_011530691.3:c.979+32G>A XP_011528993.1:n.979+32G>A
XM_017028800.1:c.979+32G>A XP_016884289.1:n.979+32G>A
XM_024452241.1:c.979+32G>A XP_024308009.1:n.979+32G>A
NM_000487.6:c.979+32G>A MANE Select NP_000478.3:n.979+32G>A
NM_001085425.3:c.979+32G>A NP_001078894.2:n.979+32G>A
NM_001085426.3:c.979+32G>A NP_001078895.2:n.979+32G>A
NM_001085427.3:c.979+32G>A NP_001078896.2:n.979+32G>A
NM_001085428.3:c.721+32G>A NP_001078897.1:n.721+32G>A
NM_001362782.2:c.721+32G>A NP_001349711.1:n.721+32G>A