Canonical Allele Identifier: CA1346017930

Gene: SYN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12139887_12139903delinsCATAAAAATATCTGCTT , CM000665.2:g.12139887_12139903delinsCATAAAAATATCTGCTT	GRCh38
NC_000003.11:g.12181387_12181403delinsCATAAAAATATCTGCTT , CM000665.1:g.12181387_12181403delinsCATAAAAATATCTGCTT	GRCh37
NC_000003.10:g.12156387_12156403delinsCATAAAAATATCTGCTT	NCBI36
NG_011728.2:g.140500_140516delinsCATAAAAATATCTGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.378-764_378-748delinsCATAAAAATATCTGCTT MANE Select	ENSP00000480050.1:n.378-764_378-748delinsCATAAAAATATCTGCTT
ENST00000424884.1:n.127-764_127-748delinsCATAAAAATATCTGCTT
ENST00000620175.4:c.378-764_378-748delinsCATAAAAATATCTGCTT	ENSP00000484916.1:n.378-764_378-748delinsCATAAAAATATCTGCTT
ENST00000621198.4:c.378-764_378-748delinsCATAAAAATATCTGCTT	ENSP00000480050.1:n.378-764_378-748delinsCATAAAAATATCTGCTT
NM_003178.5:c.378-764_378-748delinsCATAAAAATATCTGCTT	NP_003169.2:n.378-764_378-748delinsCATAAAAATATCTGCTT
NM_133625.4:c.378-764_378-748delinsCATAAAAATATCTGCTT	NP_598328.1:n.378-764_378-748delinsCATAAAAATATCTGCTT
XM_006713311.2:c.378-764_378-748delinsCATAAAAATATCTGCTT	XP_006713374.1:n.378-764_378-748delinsCATAAAAATATCTGCTT
XM_006713311.3:c.378-764_378-748delinsCATAAAAATATCTGCTT	XP_006713374.1:n.378-764_378-748delinsCATAAAAATATCTGCTT
XR_001740240.1:n.564-764_564-748delinsCATAAAAATATCTGCTT
NM_133625.5:c.378-764_378-748delinsCATAAAAATATCTGCTT	NP_598328.1:n.378-764_378-748delinsCATAAAAATATCTGCTT
NM_133625.6:c.378-764_378-748delinsCATAAAAATATCTGCTT MANE Select	NP_598328.1:n.378-764_378-748delinsCATAAAAATATCTGCTT
NM_003178.6:c.378-764_378-748delinsCATAAAAATATCTGCTT	NP_003169.2:n.378-764_378-748delinsCATAAAAATATCTGCTT