Canonical Allele Identifier: CA515391142

Gene: ARSA

Linked Data

• MyVariant Identifiers: chr22:g.51065126A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50626698A>G , CM000684.2:g.50626698A>G	GRCh38
NC_000022.10:g.51065126A>G , CM000684.1:g.51065126A>G	GRCh37
NC_000022.9:g.49411992A>G	NCBI36
NG_009260.2:g.6482T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216124.10:c.747T>C MANE Select	ENSP00000216124.5:p.Phe249=
ENST00000216124.9:c.747T>C	ENSP00000216124.5:p.Phe249=
ENST00000356098.9:c.747T>C	ENSP00000348406.5:p.Phe249=
ENST00000395619.3:c.747T>C	ENSP00000378981.3:p.Phe249=
ENST00000395621.7:c.747T>C	ENSP00000378983.3:p.Phe249=
ENST00000453344.6:c.489T>C	ENSP00000412542.2:p.Phe163=
ENST00000551731.1:n.1324T>C
NM_000487.5:c.747T>C	NP_000478.3:p.Phe249=
NM_001085425.2:c.747T>C	NP_001078894.2:p.Phe249=
NM_001085426.2:c.747T>C	NP_001078895.2:p.Phe249=
NM_001085427.2:c.747T>C	NP_001078896.2:p.Phe249=
NM_001085428.2:c.489T>C	NP_001078897.1:p.Phe163=
XM_011530690.1:c.489T>C	XP_011528992.1:p.Phe163=
XM_011530691.1:c.747T>C	XP_011528993.1:p.Phe249=
NM_001362782.1:c.489T>C	NP_001349711.1:p.Phe163=
XM_011530691.3:c.747T>C	XP_011528993.1:p.Phe249=
XM_017028800.1:c.747T>C	XP_016884289.1:p.Phe249=
XM_024452241.1:c.747T>C	XP_024308009.1:p.Phe249=
NM_000487.6:c.747T>C MANE Select	NP_000478.3:p.Phe249=
NM_001085425.3:c.747T>C	NP_001078894.2:p.Phe249=
NM_001085426.3:c.747T>C	NP_001078895.2:p.Phe249=
NM_001085427.3:c.747T>C	NP_001078896.2:p.Phe249=
NM_001085428.3:c.489T>C	NP_001078897.1:p.Phe163=
NM_001362782.2:c.489T>C	NP_001349711.1:p.Phe163=