Canonical Allele Identifier: CA2410959319
Gene: ARSA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50626934_50626935delinsCA , CM000684.2:g.50626934_50626935delinsCA GRCh38
NC_000022.10:g.51065362_51065363delinsCA , CM000684.1:g.51065362_51065363delinsCA GRCh37
NC_000022.9:g.49412228_49412229delinsCA NCBI36
NG_009260.2:g.6245_6246delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000216124.10:c.583_584delinsTG MANE Select ENSP00000216124.5:p.Trp195=
ENST00000216124.9:c.583_584delinsTG ENSP00000216124.5:p.Trp195=
ENST00000356098.9:c.583_584delinsTG ENSP00000348406.5:p.Trp195=
ENST00000395619.3:c.583_584delinsTG ENSP00000378981.3:p.Trp195=
ENST00000395621.7:c.583_584delinsTG ENSP00000378983.3:p.Trp195=
ENST00000453344.6:c.325_326delinsTG ENSP00000412542.2:p.Trp109=
ENST00000551731.1:n.1087_1088delinsTG
NM_000487.5:c.583_584delinsTG NP_000478.3:p.Trp195=
NM_001085425.2:c.583_584delinsTG NP_001078894.2:p.Trp195=
NM_001085426.2:c.583_584delinsTG NP_001078895.2:p.Trp195=
NM_001085427.2:c.583_584delinsTG NP_001078896.2:p.Trp195=
NM_001085428.2:c.325_326delinsTG NP_001078897.1:p.Trp109=
XM_011530690.1:c.325_326delinsTG XP_011528992.1:p.Trp109=
XM_011530691.1:c.583_584delinsTG XP_011528993.1:p.Trp195=
NM_001362782.1:c.325_326delinsTG NP_001349711.1:p.Trp109=
XM_011530691.3:c.583_584delinsTG XP_011528993.1:p.Trp195=
XM_017028800.1:c.583_584delinsTG XP_016884289.1:p.Trp195=
XM_024452241.1:c.583_584delinsTG XP_024308009.1:p.Trp195=
NM_000487.6:c.583_584delinsTG MANE Select NP_000478.3:p.Trp195=
NM_001085425.3:c.583_584delinsTG NP_001078894.2:p.Trp195=
NM_001085426.3:c.583_584delinsTG NP_001078895.2:p.Trp195=
NM_001085427.3:c.583_584delinsTG NP_001078896.2:p.Trp195=
NM_001085428.3:c.325_326delinsTG NP_001078897.1:p.Trp109=
NM_001362782.2:c.325_326delinsTG NP_001349711.1:p.Trp109=