Canonical Allele Identifier: CA1346039330
Gene: SYN2 HGNC NCBI

Linked Data

dbSNP Id: rs1698380855
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.12188033_12188034insC , CM000665.2:g.12188033_12188034insC GRCh38
NC_000003.11:g.12229533_12229534insC , CM000665.1:g.12229533_12229534insC GRCh37
NC_000003.10:g.12204533_12204534insC NCBI36
NG_011728.2:g.188646_188647insC

Transcript Alleles

HGVS Amino-acid change
ENST00000621198.5:c.1613+421_1613+422insC MANE Select ENSP00000480050.1:n.1613+421_1613+422insC...
ENST00000439861.5:n.1232+421_1232+422insC
ENST00000621198.4:c.1613+421_1613+422insC ENSP00000480050.1:n.1613+421_1613+422insC...
NM_133625.4:c.1613+421_1613+422insC NP_598328.1:n.1613+421_1613+422insC
XM_006713312.2:c.1130+421_1130+422insC XP_006713375.1:n.1130+421_1130+422insC
XM_006713313.2:c.842+421_842+422insC XP_006713376.1:n.842+421_842+422insC
XM_006713312.4:c.1130+421_1130+422insC XP_006713375.1:n.1130+421_1130+422insC
XM_017007087.1:c.941+421_941+422insC XP_016862576.1:n.941+421_941+422insC
NM_133625.5:c.1613+421_1613+422insC NP_598328.1:n.1613+421_1613+422insC
NM_133625.6:c.1613+421_1613+422insC MANE Select NP_598328.1:n.1613+421_1613+422insC
Search 100 bp 5'
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