Canonical Allele Identifier: CA1346017952

Gene: SYN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12139926_12139928delinsCAG , CM000665.2:g.12139926_12139928delinsCAG	GRCh38
NC_000003.11:g.12181426_12181428delinsCAG , CM000665.1:g.12181426_12181428delinsCAG	GRCh37
NC_000003.10:g.12156426_12156428delinsCAG	NCBI36
NG_011728.2:g.140539_140541delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.378-725_378-723delinsCAG MANE Select	ENSP00000480050.1:n.378-725_378-723delinsCAG
ENST00000424884.1:n.127-725_127-723delinsCAG
ENST00000620175.4:c.378-725_378-723delinsCAG	ENSP00000484916.1:n.378-725_378-723delinsCAG
ENST00000621198.4:c.378-725_378-723delinsCAG	ENSP00000480050.1:n.378-725_378-723delinsCAG
NM_003178.5:c.378-725_378-723delinsCAG	NP_003169.2:n.378-725_378-723delinsCAG
NM_133625.4:c.378-725_378-723delinsCAG	NP_598328.1:n.378-725_378-723delinsCAG
XM_006713311.2:c.378-725_378-723delinsCAG	XP_006713374.1:n.378-725_378-723delinsCAG
XM_006713311.3:c.378-725_378-723delinsCAG	XP_006713374.1:n.378-725_378-723delinsCAG
XR_001740240.1:n.564-725_564-723delinsCAG
NM_133625.5:c.378-725_378-723delinsCAG	NP_598328.1:n.378-725_378-723delinsCAG
NM_133625.6:c.378-725_378-723delinsCAG MANE Select	NP_598328.1:n.378-725_378-723delinsCAG
NM_003178.6:c.378-725_378-723delinsCAG	NP_003169.2:n.378-725_378-723delinsCAG