Canonical Allele Identifier: CA2427970781
Gene: SYN1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47572862T= , CM000685.2:g.47572862T= GRCh38
NC_000023.10:g.47432261T= , CM000685.1:g.47432261T= GRCh37
NC_000023.9:g.47317205T= NCBI36
NG_008437.1:g.51996A=
NG_016339.1:g.16746T=
NG_016339.2:g.16746T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295987.13:c.*2A= MANE Select ENSP00000295987.7:n.*2A=
ENST00000340666.5:c.*72A= ENSP00000343206.4:n.*72A=
ENST00000640721.1:c.170A= ENSP00000492857.1:n.170A=
ENST00000295987.11:c.*2A= ENSP00000295987.7:n.*2A=
ENST00000340666.4:c.*72A= ENSP00000343206.4:n.*72A=
NM_006950.3:c.*2A= MANE Select NP_008881.2:n.*2A=
NM_133499.2:c.*72A= NP_598006.1:n.*72A=
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