Canonical Allele Identifier: CA412166929

Gene: ARSA

Linked Data

• ClinVar Variation Id: 1314507
• ClinVar RCV Id: RCV001773016
• dbSNP Id: rs1196939207
• gnomAD v4: 22-50625189-T-G
• MyVariant Identifiers: chr22:g.51063617T>G (hg19) ; chr22:g.50625189T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50625189T>G , CM000684.2:g.50625189T>G	GRCh38
NC_000022.10:g.51063617T>G , CM000684.1:g.51063617T>G	GRCh37
NC_000022.9:g.49410483T>G	NCBI36
NG_009260.2:g.7991A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000216124.10:c.1486A>C MANE Select	ENSP00000216124.5:p.Thr496Pro
ENST00000216124.9:c.1486A>C	ENSP00000216124.5:p.Thr496Pro
ENST00000356098.9:c.1486A>C	ENSP00000348406.5:p.Thr496Pro
ENST00000395619.3:c.1486A>C	ENSP00000378981.3:p.Thr496Pro
ENST00000395621.7:c.1486A>C	ENSP00000378983.3:p.Thr496Pro
ENST00000453344.6:c.1228A>C	ENSP00000412542.2:p.Thr410Pro
ENST00000608497.1:c.180+174A>C
NM_000487.5:c.1486A>C	NP_000478.3:p.Thr496Pro
NM_001085425.2:c.1486A>C	NP_001078894.2:p.Thr496Pro
NM_001085426.2:c.1486A>C	NP_001078895.2:p.Thr496Pro
NM_001085427.2:c.1486A>C	NP_001078896.2:p.Thr496Pro
NM_001085428.2:c.1228A>C	NP_001078897.1:p.Thr410Pro
XM_011530690.1:c.1228A>C	XP_011528992.1:p.Thr410Pro
XM_011530691.1:c.*219A>C	XP_011528993.1:n.*219A>C
NM_001362782.1:c.1228A>C	NP_001349711.1:p.Thr410Pro
XM_011530691.3:c.*219A>C	XP_011528993.1:n.*219A>C
XM_017028800.1:c.1600A>C	XP_016884289.1:p.Thr534Pro
XM_024452241.1:c.*219A>C	XP_024308009.1:n.*219A>C
NM_000487.6:c.1486A>C MANE Select	NP_000478.3:p.Thr496Pro
NM_001085425.3:c.1486A>C	NP_001078894.2:p.Thr496Pro
NM_001085426.3:c.1486A>C	NP_001078895.2:p.Thr496Pro
NM_001085427.3:c.1486A>C	NP_001078896.2:p.Thr496Pro
NM_001085428.3:c.1228A>C	NP_001078897.1:p.Thr410Pro
NM_001362782.2:c.1228A>C	NP_001349711.1:p.Thr410Pro