Canonical Allele Identifier: CA1346017939

Gene: SYN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12139915_12139919delinsATTAC , CM000665.2:g.12139915_12139919delinsATTAC	GRCh38
NC_000003.11:g.12181415_12181419delinsATTAC , CM000665.1:g.12181415_12181419delinsATTAC	GRCh37
NC_000003.10:g.12156415_12156419delinsATTAC	NCBI36
NG_011728.2:g.140528_140532delinsATTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.378-736_378-732delinsATTAC MANE Select	ENSP00000480050.1:n.378-736_378-732delinsATTAC
ENST00000424884.1:n.127-736_127-732delinsATTAC
ENST00000620175.4:c.378-736_378-732delinsATTAC	ENSP00000484916.1:n.378-736_378-732delinsATTAC
ENST00000621198.4:c.378-736_378-732delinsATTAC	ENSP00000480050.1:n.378-736_378-732delinsATTAC
NM_003178.5:c.378-736_378-732delinsATTAC	NP_003169.2:n.378-736_378-732delinsATTAC
NM_133625.4:c.378-736_378-732delinsATTAC	NP_598328.1:n.378-736_378-732delinsATTAC
XM_006713311.2:c.378-736_378-732delinsATTAC	XP_006713374.1:n.378-736_378-732delinsATTAC
XM_006713311.3:c.378-736_378-732delinsATTAC	XP_006713374.1:n.378-736_378-732delinsATTAC
XR_001740240.1:n.564-736_564-732delinsATTAC
NM_133625.5:c.378-736_378-732delinsATTAC	NP_598328.1:n.378-736_378-732delinsATTAC
NM_133625.6:c.378-736_378-732delinsATTAC MANE Select	NP_598328.1:n.378-736_378-732delinsATTAC
NM_003178.6:c.378-736_378-732delinsATTAC	NP_003169.2:n.378-736_378-732delinsATTAC