Canonical Allele Identifier: CA2819315645

Gene: ARSA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50624265_50624266insAGAA , CM000684.2:g.50624265_50624266insAGAA	GRCh38
NC_000022.10:g.51062693_51062694insAGAA , CM000684.1:g.51062693_51062694insAGAA	GRCh37
NC_000022.9:g.49409559_49409560insAGAA	NCBI36
NG_009260.2:g.8914_8915insTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216124.10:c.*879_*880insTTCT MANE Select	ENSP00000216124.5:n.*879_*880insTTCT
ENST00000608497.1:c.181-371_181-370insTTCT
NM_000487.5:c.*879_*880insTTCT	NP_000478.3:n.*879_*880insTTCT
NM_001085425.2:c.*879_*880insTTCT	NP_001078894.2:n.*879_*880insTTCT
NM_001085426.2:c.*879_*880insTTCT	NP_001078895.2:n.*879_*880insTTCT
NM_001085427.2:c.*879_*880insTTCT	NP_001078896.2:n.*879_*880insTTCT
NM_001085428.2:c.*879_*880insTTCT	NP_001078897.1:n.*879_*880insTTCT
NM_001362782.1:c.*879_*880insTTCT	NP_001349711.1:n.*879_*880insTTCT
NM_000487.6:c.*879_*880insTTCT MANE Select	NP_000478.3:n.*879_*880insTTCT
NM_001085425.3:c.*879_*880insTTCT	NP_001078894.2:n.*879_*880insTTCT
NM_001085426.3:c.*879_*880insTTCT	NP_001078895.2:n.*879_*880insTTCT
NM_001085427.3:c.*879_*880insTTCT	NP_001078896.2:n.*879_*880insTTCT
NM_001085428.3:c.*879_*880insTTCT	NP_001078897.1:n.*879_*880insTTCT
NM_001362782.2:c.*879_*880insTTCT	NP_001349711.1:n.*879_*880insTTCT