Canonical Allele Identifier: CA2427970900
Gene: SYN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47573275G= , CM000685.2:g.47573275G= GRCh38
NC_000023.10:g.47432674G= , CM000685.1:g.47432674G= GRCh37
NC_000023.9:g.47317618G= NCBI36
NG_008437.1:g.51583C=
NG_016339.1:g.17159G=
NG_016339.2:g.17159G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1983-276C= MANE Select ENSP00000295987.7:n.1983-276C=
ENST00000340666.5:c.1983-314C= ENSP00000343206.4:n.1983-314C=
ENST00000640721.1:c.71-314C= ENSP00000492857.1:n.71-314C=
ENST00000295987.11:c.1983-276C= ENSP00000295987.7:n.1983-276C=
ENST00000340666.4:c.1983-314C= ENSP00000343206.4:n.1983-314C=
NM_006950.3:c.1983-276C= MANE Select NP_008881.2:n.1983-276C=
NM_133499.2:c.1983-314C= NP_598006.1:n.1983-314C=
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