Canonical Allele Identifier: CA412820664
Gene: SYN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.47432360T>C (hg19) chrX:g.47572961T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47572961T>C , CM000685.2:g.47572961T>C GRCh38
NC_000023.10:g.47432360T>C , CM000685.1:g.47432360T>C GRCh37
NC_000023.9:g.47317304T>C NCBI36
NG_008437.1:g.51897A>G
NG_016339.1:g.16845T>C
NG_016339.2:g.16845T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000295987.13:c.2021A>G MANE Select ENSP00000295987.7:p.Glu674Gly
ENST00000340666.5:c.1983A>G ENSP00000343206.4:p.Lys661=
ENST00000640721.1:c.71A>G ENSP00000492857.1:p.Glu24Gly
ENST00000295987.11:c.2021A>G ENSP00000295987.7:p.Glu674Gly
ENST00000340666.4:c.1983A>G ENSP00000343206.4:p.Lys661=
NM_006950.3:c.2021A>G MANE Select NP_008881.2:p.Glu674Gly
NM_133499.2:c.1983A>G NP_598006.1:p.Lys661=
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