Canonical Allele Identifier: CA2693584579
Gene: SYN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47574027dup , CM000685.2:g.47574027dup GRCh38
NC_000023.10:g.47433426dup , CM000685.1:g.47433426dup GRCh37
NC_000023.9:g.47318370dup NCBI36
NG_008437.1:g.50835dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1961dup MANE Select ENSP00000295987.7:p.Pro655ThrfsTer29
ENST00000340666.5:c.1961dup ENSP00000343206.4:p.Pro655ThrfsTer21
ENST00000640721.1:c.70+665dup ENSP00000492857.1:n.70+665dup
ENST00000295987.11:c.1961dup ENSP00000295987.7:p.Pro655ThrfsTer29
ENST00000340666.4:c.1961dup ENSP00000343206.4:p.Pro655ThrfsTer21
NM_006950.3:c.1961dup MANE Select NP_008881.2:p.Pro655ThrfsTer29
NM_133499.2:c.1961dup NP_598006.1:p.Pro655ThrfsTer21