Canonical Allele Identifier: CA412820232
Gene: SYN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.47432270G>T (hg19) chrX:g.47572871G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47572871G>T , CM000685.2:g.47572871G>T GRCh38
NC_000023.10:g.47432270G>T , CM000685.1:g.47432270G>T GRCh37
NC_000023.9:g.47317214G>T NCBI36
NG_008437.1:g.51987C>A
NG_016339.1:g.16755G>T
NG_016339.2:g.16755G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295987.13:c.2111C>A MANE Select ENSP00000295987.7:p.Ser704Tyr
ENST00000340666.5:c.*63C>A ENSP00000343206.4:n.*63C>A
ENST00000640721.1:c.161C>A ENSP00000492857.1:p.Ser54Tyr
ENST00000295987.11:c.2111C>A ENSP00000295987.7:p.Ser704Tyr
ENST00000340666.4:c.*63C>A ENSP00000343206.4:n.*63C>A
NM_006950.3:c.2111C>A MANE Select NP_008881.2:p.Ser704Tyr
NM_133499.2:c.*63C>A NP_598006.1:n.*63C>A
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