Canonical Allele Identifier: CA1346017940

Gene: SYN2

Linked Data

• dbSNP Id: rs1696976331

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12139919_12139922del , CM000665.2:g.12139919_12139922del	GRCh38
NC_000003.11:g.12181419_12181422del , CM000665.1:g.12181419_12181422del	GRCh37
NC_000003.10:g.12156419_12156422del	NCBI36
NG_011728.2:g.140532_140535del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.378-732_378-729del MANE Select	ENSP00000480050.1:n.378-732_378-729del
ENST00000424884.1:n.127-732_127-729del
ENST00000620175.4:c.378-732_378-729del	ENSP00000484916.1:n.378-732_378-729del
ENST00000621198.4:c.378-732_378-729del	ENSP00000480050.1:n.378-732_378-729del
NM_003178.5:c.378-732_378-729del	NP_003169.2:n.378-732_378-729del
NM_133625.4:c.378-732_378-729del	NP_598328.1:n.378-732_378-729del
XM_006713311.2:c.378-732_378-729del	XP_006713374.1:n.378-732_378-729del
XM_006713311.3:c.378-732_378-729del	XP_006713374.1:n.378-732_378-729del
XR_001740240.1:n.564-732_564-729del
NM_133625.5:c.378-732_378-729del	NP_598328.1:n.378-732_378-729del
NM_133625.6:c.378-732_378-729del MANE Select	NP_598328.1:n.378-732_378-729del
NM_003178.6:c.378-732_378-729del	NP_003169.2:n.378-732_378-729del