Canonical Allele Identifier: CA2427976102
Gene: SYN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47588477G= , CM000685.2:g.47588477G= GRCh38
NC_000023.10:g.47447876G= , CM000685.1:g.47447876G= GRCh37
NC_000023.9:g.47332820G= NCBI36
NG_008437.1:g.36381C=
NG_012533.1:g.11187G=

Transcript Alleles

HGVS Amino-acid change
ENST00000295987.13:c.775-10976C= MANE Select ENSP00000295987.7:n.775-10976C=
ENST00000340666.5:c.775-10976C= ENSP00000343206.4:n.775-10976C=
ENST00000295987.11:c.775-10976C= ENSP00000295987.7:n.775-10976C=
ENST00000340666.4:c.775-10976C= ENSP00000343206.4:n.775-10976C=
NM_006950.3:c.775-10976C= MANE Select NP_008881.2:n.775-10976C=
NM_133499.2:c.775-10976C= NP_598006.1:n.775-10976C=
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