Canonical Allele Identifier: CA2657593847
Gene: ARSA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50627218_50627219insC , CM000684.2:g.50627218_50627219insC GRCh38
NC_000022.10:g.51065646_51065647insC , CM000684.1:g.51065646_51065647insC GRCh37
NC_000022.9:g.49412512_49412513insC NCBI36
NG_009260.2:g.5961_5962insG

Transcript Alleles

HGVS Amino-acid change
ENST00000216124.10:c.412_413insG MANE Select ENSP00000216124.5:p.Pro138ArgfsTer?
ENST00000216124.9:c.412_413insG ENSP00000216124.5:p.Pro138ArgfsTer?
ENST00000356098.9:c.412_413insG ENSP00000348406.5:p.Pro138ArgfsTer?
ENST00000395619.3:c.412_413insG ENSP00000378981.3:p.Pro138ArgfsTer?
ENST00000395621.7:c.412_413insG ENSP00000378983.3:p.Pro138ArgfsTer?
ENST00000453344.6:c.154_155insG ENSP00000412542.2:p.Pro52ArgfsTer?
ENST00000551731.1:n.803_804insG
NM_000487.5:c.412_413insG NP_000478.3:p.Pro138ArgfsTer?
NM_001085425.2:c.412_413insG NP_001078894.2:p.Pro138ArgfsTer?
NM_001085426.2:c.412_413insG NP_001078895.2:p.Pro138ArgfsTer?
NM_001085427.2:c.412_413insG NP_001078896.2:p.Pro138ArgfsTer?
NM_001085428.2:c.154_155insG NP_001078897.1:p.Pro52ArgfsTer?
XM_011530690.1:c.154_155insG XP_011528992.1:p.Pro52ArgfsTer?
XM_011530691.1:c.412_413insG XP_011528993.1:p.Pro138ArgfsTer?
NM_001362782.1:c.154_155insG NP_001349711.1:p.Pro52ArgfsTer?
XM_011530691.3:c.412_413insG XP_011528993.1:p.Pro138ArgfsTer?
XM_017028800.1:c.412_413insG XP_016884289.1:p.Pro138ArgfsTer?
XM_024452241.1:c.412_413insG XP_024308009.1:p.Pro138ArgfsTer?
NM_000487.6:c.412_413insG MANE Select NP_000478.3:p.Pro138ArgfsTer?
NM_001085425.3:c.412_413insG NP_001078894.2:p.Pro138ArgfsTer?
NM_001085426.3:c.412_413insG NP_001078895.2:p.Pro138ArgfsTer?
NM_001085427.3:c.412_413insG NP_001078896.2:p.Pro138ArgfsTer?
NM_001085428.3:c.154_155insG NP_001078897.1:p.Pro52ArgfsTer?
NM_001362782.2:c.154_155insG NP_001349711.1:p.Pro52ArgfsTer?