Canonical Allele Identifier: CA2427971139
Gene: SYN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47573986G= , CM000685.2:g.47573986G= GRCh38
NC_000023.10:g.47433385G= , CM000685.1:g.47433385G= GRCh37
NC_000023.9:g.47318329G= NCBI36
NG_008437.1:g.50872C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1982+16C= MANE Select ENSP00000295987.7:n.1982+16C=
ENST00000340666.5:c.1982+16C= ENSP00000343206.4:n.1982+16C=
ENST00000640721.1:c.70+702C= ENSP00000492857.1:n.70+702C=
ENST00000295987.11:c.1982+16C= ENSP00000295987.7:n.1982+16C=
ENST00000340666.4:c.1982+16C= ENSP00000343206.4:n.1982+16C=
NM_006950.3:c.1982+16C= MANE Select NP_008881.2:n.1982+16C=
NM_133499.2:c.1982+16C= NP_598006.1:n.1982+16C=
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