Canonical Allele Identifier: CA2427976135
Gene: SYN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47588572G= , CM000685.2:g.47588572G= GRCh38
NC_000023.10:g.47447971G= , CM000685.1:g.47447971G= GRCh37
NC_000023.9:g.47332915G= NCBI36
NG_008437.1:g.36286C=
NG_012533.1:g.11282G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.775-11071C= MANE Select ENSP00000295987.7:n.775-11071C=
ENST00000340666.5:c.775-11071C= ENSP00000343206.4:n.775-11071C=
ENST00000295987.11:c.775-11071C= ENSP00000295987.7:n.775-11071C=
ENST00000340666.4:c.775-11071C= ENSP00000343206.4:n.775-11071C=
NM_006950.3:c.775-11071C= MANE Select NP_008881.2:n.775-11071C=
NM_133499.2:c.775-11071C= NP_598006.1:n.775-11071C=