Canonical Allele Identifier: CA916835843
Gene: SYN2 HGNC NCBI

Linked Data

dbSNP Id: rs1553624091
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12188017del , CM000665.2:g.12188017del GRCh38
NC_000003.11:g.12229517del , CM000665.1:g.12229517del GRCh37
NC_000003.10:g.12204517del NCBI36
NG_011728.2:g.188630del

Transcript Alleles

HGVS Amino-acid change
ENST00000621198.5:c.1613+405del MANE Select ENSP00000480050.1:n.1613+405del
ENST00000439861.5:n.1232+405del
ENST00000621198.4:c.1613+405del ENSP00000480050.1:n.1613+405del
NM_133625.4:c.1613+405del NP_598328.1:n.1613+405del
XM_006713312.2:c.1130+405del XP_006713375.1:n.1130+405del
XM_006713313.2:c.842+405del XP_006713376.1:n.842+405del
XM_006713312.4:c.1130+405del XP_006713375.1:n.1130+405del
XM_017007087.1:c.941+405del XP_016862576.1:n.941+405del
NM_133625.5:c.1613+405del NP_598328.1:n.1613+405del
NM_133625.6:c.1613+405del MANE Select NP_598328.1:n.1613+405del
Search 100 bp 5'
Search 100 bp 3'