Canonical Allele Identifier: CA1346018008

Gene: SYN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12140005_12140010delinsCACCTT , CM000665.2:g.12140005_12140010delinsCACCTT	GRCh38
NC_000003.11:g.12181505_12181510delinsCACCTT , CM000665.1:g.12181505_12181510delinsCACCTT	GRCh37
NC_000003.10:g.12156505_12156510delinsCACCTT	NCBI36
NG_011728.2:g.140618_140623delinsCACCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.378-646_378-641delinsCACCTT MANE Select	ENSP00000480050.1:n.378-646_378-641delinsCACCTT
ENST00000424884.1:n.127-646_127-641delinsCACCTT
ENST00000620175.4:c.378-646_378-641delinsCACCTT	ENSP00000484916.1:n.378-646_378-641delinsCACCTT
ENST00000621198.4:c.378-646_378-641delinsCACCTT	ENSP00000480050.1:n.378-646_378-641delinsCACCTT
NM_003178.5:c.378-646_378-641delinsCACCTT	NP_003169.2:n.378-646_378-641delinsCACCTT
NM_133625.4:c.378-646_378-641delinsCACCTT	NP_598328.1:n.378-646_378-641delinsCACCTT
XM_006713311.2:c.378-646_378-641delinsCACCTT	XP_006713374.1:n.378-646_378-641delinsCACCTT
XM_006713311.3:c.378-646_378-641delinsCACCTT	XP_006713374.1:n.378-646_378-641delinsCACCTT
XR_001740240.1:n.564-646_564-641delinsCACCTT
NM_133625.5:c.378-646_378-641delinsCACCTT	NP_598328.1:n.378-646_378-641delinsCACCTT
NM_133625.6:c.378-646_378-641delinsCACCTT MANE Select	NP_598328.1:n.378-646_378-641delinsCACCTT
NM_003178.6:c.378-646_378-641delinsCACCTT	NP_003169.2:n.378-646_378-641delinsCACCTT