Canonical Allele Identifier: CA412822745
Gene: SYN1 HGNC NCBI

Linked Data

dbSNP Id: rs1327204390
gnomAD v2: X-47433648-C-T
gnomAD v4: X-47574249-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47574249C>T , CM000685.2:g.47574249C>T GRCh38
NC_000023.10:g.47433648C>T , CM000685.1:g.47433648C>T GRCh37
NC_000023.9:g.47318592C>T NCBI36
NG_008437.1:g.50609G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1735G>A MANE Select ENSP00000295987.7:p.Gly579Arg
ENST00000340666.5:c.1735G>A ENSP00000343206.4:p.Gly579Arg
ENST00000640721.1:c.70+439G>A ENSP00000492857.1:n.70+439G>A
ENST00000295987.11:c.1735G>A ENSP00000295987.7:p.Gly579Arg
ENST00000340666.4:c.1735G>A ENSP00000343206.4:p.Gly579Arg
NM_006950.3:c.1735G>A MANE Select NP_008881.2:p.Gly579Arg
NM_133499.2:c.1735G>A NP_598006.1:p.Gly579Arg