Canonical Allele Identifier: CA1346018114

Gene: SYN2

Linked Data

• dbSNP Id: rs1696982162

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12140224_12140226del , CM000665.2:g.12140224_12140226del	GRCh38
NC_000003.11:g.12181724_12181726del , CM000665.1:g.12181724_12181726del	GRCh37
NC_000003.10:g.12156724_12156726del	NCBI36
NG_011728.2:g.140837_140839del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.378-427_378-425del MANE Select	ENSP00000480050.1:n.378-427_378-425del
ENST00000424884.1:n.127-427_127-425del
ENST00000620175.4:c.378-427_378-425del	ENSP00000484916.1:n.378-427_378-425del
ENST00000621198.4:c.378-427_378-425del	ENSP00000480050.1:n.378-427_378-425del
NM_003178.5:c.378-427_378-425del	NP_003169.2:n.378-427_378-425del
NM_133625.4:c.378-427_378-425del	NP_598328.1:n.378-427_378-425del
XM_006713311.2:c.378-427_378-425del	XP_006713374.1:n.378-427_378-425del
XM_006713311.3:c.378-427_378-425del	XP_006713374.1:n.378-427_378-425del
XR_001740240.1:n.564-427_564-425del
NM_133625.5:c.378-427_378-425del	NP_598328.1:n.378-427_378-425del
NM_133625.6:c.378-427_378-425del MANE Select	NP_598328.1:n.378-427_378-425del
NM_003178.6:c.378-427_378-425del	NP_003169.2:n.378-427_378-425del