Canonical Allele Identifier: CA2573129239
Gene: SYN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47588546G>C , CM000685.2:g.47588546G>C GRCh38
NC_000023.10:g.47447945G>C , CM000685.1:g.47447945G>C GRCh37
NC_000023.9:g.47332889G>C NCBI36
NG_008437.1:g.36312C>G
NG_012533.1:g.11256G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.775-11045C>G MANE Select ENSP00000295987.7:n.775-11045C>G
ENST00000340666.5:c.775-11045C>G ENSP00000343206.4:n.775-11045C>G
ENST00000295987.11:c.775-11045C>G ENSP00000295987.7:n.775-11045C>G
ENST00000340666.4:c.775-11045C>G ENSP00000343206.4:n.775-11045C>G
NM_006950.3:c.775-11045C>G MANE Select NP_008881.2:n.775-11045C>G
NM_133499.2:c.775-11045C>G NP_598006.1:n.775-11045C>G
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