Canonical Allele Identifier: CA1346039316
Gene: SYN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12188016_12188017delinsTC , CM000665.2:g.12188016_12188017delinsTC GRCh38
NC_000003.11:g.12229516_12229517delinsTC , CM000665.1:g.12229516_12229517delinsTC GRCh37
NC_000003.10:g.12204516_12204517delinsTC NCBI36
NG_011728.2:g.188629_188630delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000621198.5:c.1613+404_1613+405delinsTC MANE Select ENSP00000480050.1:n.1613+404_1613+405deli...
ENST00000439861.5:n.1232+404_1232+405delinsTC
ENST00000621198.4:c.1613+404_1613+405delinsTC ENSP00000480050.1:n.1613+404_1613+405deli...
NM_133625.4:c.1613+404_1613+405delinsTC NP_598328.1:n.1613+404_1613+405delinsTC
XM_006713312.2:c.1130+404_1130+405delinsTC XP_006713375.1:n.1130+404_1130+405delinsT...
XM_006713313.2:c.842+404_842+405delinsTC XP_006713376.1:n.842+404_842+405delinsTC
XM_006713312.4:c.1130+404_1130+405delinsTC XP_006713375.1:n.1130+404_1130+405delinsT...
XM_017007087.1:c.941+404_941+405delinsTC XP_016862576.1:n.941+404_941+405delinsTC
NM_133625.5:c.1613+404_1613+405delinsTC NP_598328.1:n.1613+404_1613+405delinsTC
NM_133625.6:c.1613+404_1613+405delinsTC MANE Select NP_598328.1:n.1613+404_1613+405delinsTC
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