Canonical Allele Identifier: CA2410958555
Gene: ARSA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50625558G= , CM000684.2:g.50625558G= GRCh38
NC_000022.10:g.51063986G= , CM000684.1:g.51063986G= GRCh37
NC_000022.9:g.49410852G= NCBI36
NG_009260.2:g.7622C=

Transcript Alleles

HGVS Amino-acid change
ENST00000216124.10:c.1210+21C= MANE Select ENSP00000216124.5:n.1210+21C=
ENST00000216124.9:c.1210+21C= ENSP00000216124.5:n.1210+21C=
ENST00000356098.9:c.1210+21C= ENSP00000348406.5:n.1210+21C=
ENST00000395619.3:c.1210+21C= ENSP00000378981.3:n.1210+21C=
ENST00000395621.7:c.1210+21C= ENSP00000378983.3:n.1210+21C=
ENST00000453344.6:c.952+21C= ENSP00000412542.2:n.952+21C=
ENST00000608497.1:c.78+21C=
NM_000487.5:c.1210+21C= NP_000478.3:n.1210+21C=
NM_001085425.2:c.1210+21C= NP_001078894.2:n.1210+21C=
NM_001085426.2:c.1210+21C= NP_001078895.2:n.1210+21C=
NM_001085427.2:c.1210+21C= NP_001078896.2:n.1210+21C=
NM_001085428.2:c.952+21C= NP_001078897.1:n.952+21C=
XM_011530690.1:c.952+21C= XP_011528992.1:n.952+21C=
XM_011530691.1:c.1108-94C= XP_011528993.1:n.1108-94C=
NM_001362782.1:c.952+21C= NP_001349711.1:n.952+21C=
XM_011530691.3:c.1108-94C= XP_011528993.1:n.1108-94C=
XM_017028800.1:c.1231C= XP_016884289.1:p.Pro411=
XM_024452241.1:c.1108-94C= XP_024308009.1:n.1108-94C=
NM_000487.6:c.1210+21C= MANE Select NP_000478.3:n.1210+21C=
NM_001085425.3:c.1210+21C= NP_001078894.2:n.1210+21C=
NM_001085426.3:c.1210+21C= NP_001078895.2:n.1210+21C=
NM_001085427.3:c.1210+21C= NP_001078896.2:n.1210+21C=
NM_001085428.3:c.952+21C= NP_001078897.1:n.952+21C=
NM_001362782.2:c.952+21C= NP_001349711.1:n.952+21C=