Canonical Allele Identifier: CA2410957903

Gene: ARSA

Linked Data

• dbSNP Id: rs2082629220

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50624295T>A , CM000684.2:g.50624295T>A	GRCh38
NC_000022.10:g.51062723T>A , CM000684.1:g.51062723T>A	GRCh37
NC_000022.9:g.49409589T>A	NCBI36
NG_009260.2:g.8885A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216124.10:c.*850A>T MANE Select	ENSP00000216124.5:n.*850A>T
ENST00000608497.1:c.181-400A>T
NM_000487.5:c.*850A>T	NP_000478.3:n.*850A>T
NM_001085425.2:c.*850A>T	NP_001078894.2:n.*850A>T
NM_001085426.2:c.*850A>T	NP_001078895.2:n.*850A>T
NM_001085427.2:c.*850A>T	NP_001078896.2:n.*850A>T
NM_001085428.2:c.*850A>T	NP_001078897.1:n.*850A>T
NM_001362782.1:c.*850A>T	NP_001349711.1:n.*850A>T
NM_000487.6:c.*850A>T MANE Select	NP_000478.3:n.*850A>T
NM_001085425.3:c.*850A>T	NP_001078894.2:n.*850A>T
NM_001085426.3:c.*850A>T	NP_001078895.2:n.*850A>T
NM_001085427.3:c.*850A>T	NP_001078896.2:n.*850A>T
NM_001085428.3:c.*850A>T	NP_001078897.1:n.*850A>T
NM_001362782.2:c.*850A>T	NP_001349711.1:n.*850A>T