Canonical Allele Identifier: CA2839660352

Gene: ARSA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50627128del , CM000684.2:g.50627128del	GRCh38
NC_000022.10:g.51065556del , CM000684.1:g.51065556del	GRCh37
NC_000022.9:g.49412422del	NCBI36
NG_009260.2:g.6054del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216124.10:c.465+40del MANE Select	ENSP00000216124.5:n.465+40del
ENST00000216124.9:c.465+40del	ENSP00000216124.5:n.465+40del
ENST00000356098.9:c.465+40del	ENSP00000348406.5:n.465+40del
ENST00000395619.3:c.465+40del	ENSP00000378981.3:n.465+40del
ENST00000395621.7:c.465+40del	ENSP00000378983.3:n.465+40del
ENST00000453344.6:c.207+40del	ENSP00000412542.2:n.207+40del
ENST00000551731.1:n.896del
NM_000487.5:c.465+40del	NP_000478.3:n.465+40del
NM_001085425.2:c.465+40del	NP_001078894.2:n.465+40del
NM_001085426.2:c.465+40del	NP_001078895.2:n.465+40del
NM_001085427.2:c.465+40del	NP_001078896.2:n.465+40del
NM_001085428.2:c.207+40del	NP_001078897.1:n.207+40del
XM_011530690.1:c.207+40del	XP_011528992.1:n.207+40del
XM_011530691.1:c.465+40del	XP_011528993.1:n.465+40del
NM_001362782.1:c.207+40del	NP_001349711.1:n.207+40del
XM_011530691.3:c.465+40del	XP_011528993.1:n.465+40del
XM_017028800.1:c.465+40del	XP_016884289.1:n.465+40del
XM_024452241.1:c.465+40del	XP_024308009.1:n.465+40del
NM_000487.6:c.465+40del MANE Select	NP_000478.3:n.465+40del
NM_001085425.3:c.465+40del	NP_001078894.2:n.465+40del
NM_001085426.3:c.465+40del	NP_001078895.2:n.465+40del
NM_001085427.3:c.465+40del	NP_001078896.2:n.465+40del
NM_001085428.3:c.207+40del	NP_001078897.1:n.207+40del
NM_001362782.2:c.207+40del	NP_001349711.1:n.207+40del