Canonical Allele Identifier: CA2657592637

Gene: ARSA

Linked Data

• gnomAD v4: 22-50626290-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50626291del , CM000684.2:g.50626291del	GRCh38
NC_000022.10:g.51064719del , CM000684.1:g.51064719del	GRCh37
NC_000022.9:g.49411585del	NCBI36
NG_009260.2:g.6889del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216124.10:c.855-13del MANE Select	ENSP00000216124.5:n.855-13del
ENST00000216124.9:c.855-13del	ENSP00000216124.5:n.855-13del
ENST00000356098.9:c.855-13del	ENSP00000348406.5:n.855-13del
ENST00000395619.3:c.855-13del	ENSP00000378981.3:n.855-13del
ENST00000395621.7:c.855-13del	ENSP00000378983.3:n.855-13del
ENST00000453344.6:c.597-13del	ENSP00000412542.2:n.597-13del
NM_000487.5:c.855-13del	NP_000478.3:n.855-13del
NM_001085425.2:c.855-13del	NP_001078894.2:n.855-13del
NM_001085426.2:c.855-13del	NP_001078895.2:n.855-13del
NM_001085427.2:c.855-13del	NP_001078896.2:n.855-13del
NM_001085428.2:c.597-13del	NP_001078897.1:n.597-13del
XM_011530690.1:c.597-13del	XP_011528992.1:n.597-13del
XM_011530691.1:c.855-13del	XP_011528993.1:n.855-13del
NM_001362782.1:c.597-13del	NP_001349711.1:n.597-13del
XM_011530691.3:c.855-13del	XP_011528993.1:n.855-13del
XM_017028800.1:c.855-13del	XP_016884289.1:n.855-13del
XM_024452241.1:c.855-13del	XP_024308009.1:n.855-13del
NM_000487.6:c.855-13del MANE Select	NP_000478.3:n.855-13del
NM_001085425.3:c.855-13del	NP_001078894.2:n.855-13del
NM_001085426.3:c.855-13del	NP_001078895.2:n.855-13del
NM_001085427.3:c.855-13del	NP_001078896.2:n.855-13del
NM_001085428.3:c.597-13del	NP_001078897.1:n.597-13del
NM_001362782.2:c.597-13del	NP_001349711.1:n.597-13del