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Canonical Allele Identifier: Get Identifier
Gene: SNCA HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Transcript change
ENSP00000423445.1:p.Ala53Thr
ENST00000506691.1:c.[157G>A;160A=]

ENST00000506691.1:c.[157G>A;162A>C]

ENST00000506691.1:c.[157G>A;162A>G]

ENST00000506691.1:c.[157G>A;162A>T]

ENST00000506691.1:c.[157G>A;165G>A]

ENST00000506691.1:c.[157G>A;165G>C]

ENST00000506691.1:c.[157G>A;165G>T]

ENST00000506691.1:c.[157G>A;166G=]

ENST00000506691.1:c.[157G>A;168T>A]

ENST00000506691.1:c.[157G>A;168T>C]

ENST00000506691.1:c.[157G>A;168T>G]

ENST00000506691.1:c.[157G>A;171G>A]

ENST00000506691.1:c.[157G>A;174G>A]

ENST00000506691.1:c.[157G>A;174G=]

ENST00000506691.1:c.[157G>A;177C>A]

ENST00000506691.1:c.[157G>A;177C=]

ENST00000506691.1:c.[157G>A;177C>G]

ENST00000506691.1:c.[157G>A;177C>T]

ENST00000506691.1:c.[157G>A;180A>G]

ENST00000506691.1:c.[157G>A;183G>A]

ENST00000506691.1:c.[157G>A;183G=]

ENST00000506691.1:c.[157G>A;186A>G]

ENST00000506691.1:c.[157G>A;187G=]

ENST00000506691.1:c.[157G>A;189G>A]

ENST00000506691.1:c.[157G>A;189G>C]

ENST00000506691.1:c.[157G>A;189G=]

ENST00000506691.1:c.[157G>A;189G>T]

ENST00000506691.1:c.[157G>A;192A=]

ENST00000506691.1:c.[157G>A;192A>C]

ENST00000506691.1:c.[157G>A;192A>G]

ENST00000506691.1:c.[157G>A;192A>T]

ENST00000506691.1:c.[157G>A;195T>C]