Canonical Allele Identifier: CA2410958891
Gene: ARSA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50626170_50626178delinsTGGCCAGAA , CM000684.2:g.50626170_50626178delinsTGGCCAGAA GRCh38
NC_000022.10:g.51064598_51064606delinsTGGCCAGAA , CM000684.1:g.51064598_51064606delinsTGGCCAGAA GRCh37
NC_000022.9:g.49411464_49411472delinsTGGCCAGAA NCBI36
NG_009260.2:g.7002_7010delinsTTCTGGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000216124.10:c.955_963delinsTTCTGGCCA MANE Select ENSP00000216124.5:p.Phe319=
ENST00000216124.9:c.955_963delinsTTCTGGCCA ENSP00000216124.5:p.Phe319=
ENST00000356098.9:c.955_963delinsTTCTGGCCA ENSP00000348406.5:p.Phe319=
ENST00000395619.3:c.955_963delinsTTCTGGCCA ENSP00000378981.3:p.Phe319=
ENST00000395621.7:c.955_963delinsTTCTGGCCA ENSP00000378983.3:p.Phe319=
ENST00000453344.6:c.697_705delinsTTCTGGCCA ENSP00000412542.2:p.Phe233=
NM_000487.5:c.955_963delinsTTCTGGCCA NP_000478.3:p.Phe319=
NM_001085425.2:c.955_963delinsTTCTGGCCA NP_001078894.2:p.Phe319=
NM_001085426.2:c.955_963delinsTTCTGGCCA NP_001078895.2:p.Phe319=
NM_001085427.2:c.955_963delinsTTCTGGCCA NP_001078896.2:p.Phe319=
NM_001085428.2:c.697_705delinsTTCTGGCCA NP_001078897.1:p.Phe233=
XM_011530690.1:c.697_705delinsTTCTGGCCA XP_011528992.1:p.Phe233=
XM_011530691.1:c.955_963delinsTTCTGGCCA XP_011528993.1:p.Phe319=
NM_001362782.1:c.697_705delinsTTCTGGCCA NP_001349711.1:p.Phe233=
XM_011530691.3:c.955_963delinsTTCTGGCCA XP_011528993.1:p.Phe319=
XM_017028800.1:c.955_963delinsTTCTGGCCA XP_016884289.1:p.Phe319=
XM_024452241.1:c.955_963delinsTTCTGGCCA XP_024308009.1:p.Phe319=
NM_000487.6:c.955_963delinsTTCTGGCCA MANE Select NP_000478.3:p.Phe319=
NM_001085425.3:c.955_963delinsTTCTGGCCA NP_001078894.2:p.Phe319=
NM_001085426.3:c.955_963delinsTTCTGGCCA NP_001078895.2:p.Phe319=
NM_001085427.3:c.955_963delinsTTCTGGCCA NP_001078896.2:p.Phe319=
NM_001085428.3:c.697_705delinsTTCTGGCCA NP_001078897.1:p.Phe233=
NM_001362782.2:c.697_705delinsTTCTGGCCA NP_001349711.1:p.Phe233=