Canonical Allele Identifier: CA412823150
Gene: SYN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47574387A>C , CM000685.2:g.47574387A>C GRCh38
NC_000023.10:g.47433786A>C , CM000685.1:g.47433786A>C GRCh37
NC_000023.9:g.47318730A>C NCBI36
NG_008437.1:g.50471T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1597T>G MANE Select ENSP00000295987.7:p.Ser533Ala
ENST00000340666.5:c.1597T>G ENSP00000343206.4:p.Ser533Ala
ENST00000640721.1:c.70+301T>G ENSP00000492857.1:n.70+301T>G
ENST00000295987.11:c.1597T>G ENSP00000295987.7:p.Ser533Ala
ENST00000340666.4:c.1597T>G ENSP00000343206.4:p.Ser533Ala
NM_006950.3:c.1597T>G MANE Select NP_008881.2:p.Ser533Ala
NM_133499.2:c.1597T>G NP_598006.1:p.Ser533Ala