Canonical Allele Identifier: CA1346039320
Gene: SYN2 HGNC NCBI

Linked Data

dbSNP Id: rs1698380564
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12188017_12188025del , CM000665.2:g.12188017_12188025del GRCh38
NC_000003.11:g.12229517_12229525del , CM000665.1:g.12229517_12229525del GRCh37
NC_000003.10:g.12204517_12204525del NCBI36
NG_011728.2:g.188630_188638del

Transcript Alleles

HGVS Amino-acid change
ENST00000621198.5:c.1613+405_1613+413del MANE Select ENSP00000480050.1:n.1613+405_1613+413del
ENST00000439861.5:n.1232+405_1232+413del
ENST00000621198.4:c.1613+405_1613+413del ENSP00000480050.1:n.1613+405_1613+413del
NM_133625.4:c.1613+405_1613+413del NP_598328.1:n.1613+405_1613+413del
XM_006713312.2:c.1130+405_1130+413del XP_006713375.1:n.1130+405_1130+413del
XM_006713313.2:c.842+405_842+413del XP_006713376.1:n.842+405_842+413del
XM_006713312.4:c.1130+405_1130+413del XP_006713375.1:n.1130+405_1130+413del
XM_017007087.1:c.941+405_941+413del XP_016862576.1:n.941+405_941+413del
NM_133625.5:c.1613+405_1613+413del NP_598328.1:n.1613+405_1613+413del
NM_133625.6:c.1613+405_1613+413del MANE Select NP_598328.1:n.1613+405_1613+413del
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