Canonical Allele Identifier: CA412826559
Gene: SYN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.47435627T>G (hg19) chrX:g.47576228T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47576228T>G , CM000685.2:g.47576228T>G GRCh38
NC_000023.10:g.47435627T>G , CM000685.1:g.47435627T>G GRCh37
NC_000023.9:g.47320571T>G NCBI36
NG_008437.1:g.48630A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295987.13:c.1061A>C MANE Select ENSP00000295987.7:p.Lys354Thr
ENST00000340666.5:c.1061A>C ENSP00000343206.4:p.Lys354Thr
ENST00000295987.11:c.1061A>C ENSP00000295987.7:p.Lys354Thr
ENST00000340666.4:c.1061A>C ENSP00000343206.4:p.Lys354Thr
NM_006950.3:c.1061A>C MANE Select NP_008881.2:p.Lys354Thr
NM_133499.2:c.1061A>C NP_598006.1:p.Lys354Thr
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