Canonical Allele Identifier: CA1345988066

Gene: SYN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12075120G= , CM000665.2:g.12075120G=	GRCh38
NC_000003.11:g.12116620G= , CM000665.1:g.12116620G=	GRCh37
NC_000003.10:g.12091620G=	NCBI36
NG_011728.2:g.75733G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.378-65531G= MANE Select	ENSP00000480050.1:n.378-65531G=
ENST00000424884.1:n.126+3437G=
ENST00000620175.4:c.378-65531G=	ENSP00000484916.1:n.378-65531G=
ENST00000621198.4:c.378-65531G=	ENSP00000480050.1:n.378-65531G=
NM_003178.5:c.378-65531G=	NP_003169.2:n.378-65531G=
NM_133625.4:c.378-65531G=	NP_598328.1:n.378-65531G=
XM_006713311.2:c.378-65531G=	XP_006713374.1:n.378-65531G=
XM_006713311.3:c.378-65531G=	XP_006713374.1:n.378-65531G=
XR_001740240.1:n.564-65531G=
NM_133625.5:c.378-65531G=	NP_598328.1:n.378-65531G=
NM_133625.6:c.378-65531G= MANE Select	NP_598328.1:n.378-65531G=
NM_003178.6:c.378-65531G=	NP_003169.2:n.378-65531G=