Canonical Allele Identifier: CA10398341
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1159939
ClinVar RCV Id: RCV001503870 RCV003438843
dbSNP Id: rs201236500
ExAC: X:47433412 G / A
gnomAD v2: X-47433412-G-A
gnomAD v3: X-47574013-G-A
gnomAD v4: X-47574013-G-A
MyVariant Identifiers: chrX:g.47433412G>A (hg19) chrX:g.47574013G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47574013G>A , CM000685.2:g.47574013G>A GRCh38
NC_000023.10:g.47433412G>A , CM000685.1:g.47433412G>A GRCh37
NC_000023.9:g.47318356G>A NCBI36
NG_008437.1:g.50845C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1971C>T MANE Select ENSP00000295987.7:p.His657=
ENST00000340666.5:c.1971C>T ENSP00000343206.4:p.His657=
ENST00000640721.1:c.70+675C>T ENSP00000492857.1:n.70+675C>T
ENST00000295987.11:c.1971C>T ENSP00000295987.7:p.His657=
ENST00000340666.4:c.1971C>T ENSP00000343206.4:p.His657=
NM_006950.3:c.1971C>T MANE Select NP_008881.2:p.His657=
NM_133499.2:c.1971C>T NP_598006.1:p.His657=
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