Canonical Allele Identifier: CA2427971328
Gene: SYN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47574543A= , CM000685.2:g.47574543A= GRCh38
NC_000023.10:g.47433942A= , CM000685.1:g.47433942A= GRCh37
NC_000023.9:g.47318886A= NCBI36
NG_008437.1:g.50315T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295987.13:c.1441T= MANE Select ENSP00000295987.7:p.Leu481=
ENST00000340666.5:c.1441T= ENSP00000343206.4:p.Leu481=
ENST00000640721.1:c.70+145T= ENSP00000492857.1:n.70+145T=
ENST00000295987.11:c.1441T= ENSP00000295987.7:p.Leu481=
ENST00000340666.4:c.1441T= ENSP00000343206.4:p.Leu481=
NM_006950.3:c.1441T= MANE Select NP_008881.2:p.Leu481=
NM_133499.2:c.1441T= NP_598006.1:p.Leu481=
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Search 100 bp 3'