Canonical Allele Identifier: CA412820657
Gene: SYN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.47432359C>G (hg19) chrX:g.47572960C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47572960C>G , CM000685.2:g.47572960C>G GRCh38
NC_000023.10:g.47432359C>G , CM000685.1:g.47432359C>G GRCh37
NC_000023.9:g.47317303C>G NCBI36
NG_008437.1:g.51898G>C
NG_016339.1:g.16844C>G
NG_016339.2:g.16844C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000295987.13:c.2022G>C MANE Select ENSP00000295987.7:p.Glu674Asp
ENST00000340666.5:c.1984G>C ENSP00000343206.4:p.Ala662Pro
ENST00000640721.1:c.72G>C ENSP00000492857.1:p.Glu24Asp
ENST00000295987.11:c.2022G>C ENSP00000295987.7:p.Glu674Asp
ENST00000340666.4:c.1984G>C ENSP00000343206.4:p.Ala662Pro
NM_006950.3:c.2022G>C MANE Select NP_008881.2:p.Glu674Asp
NM_133499.2:c.1984G>C NP_598006.1:p.Ala662Pro
Search 100 bp 5'
Search 100 bp 3'