Canonical Allele Identifier: CA1346039277

Gene: SYN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12187943C= , CM000665.2:g.12187943C=	GRCh38
NC_000003.11:g.12229443C= , CM000665.1:g.12229443C=	GRCh37
NC_000003.10:g.12204443C=	NCBI36
NG_011728.2:g.188556C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.1613+331C= MANE Select	ENSP00000480050.1:n.1613+331C=
ENST00000439861.5:n.1232+331C=
ENST00000621198.4:c.1613+331C=	ENSP00000480050.1:n.1613+331C=
NM_133625.4:c.1613+331C=	NP_598328.1:n.1613+331C=
XM_006713312.2:c.1130+331C=	XP_006713375.1:n.1130+331C=
XM_006713313.2:c.842+331C=	XP_006713376.1:n.842+331C=
XM_006713312.4:c.1130+331C=	XP_006713375.1:n.1130+331C=
XM_017007087.1:c.941+331C=	XP_016862576.1:n.941+331C=
NM_133625.5:c.1613+331C=	NP_598328.1:n.1613+331C=
NM_133625.6:c.1613+331C= MANE Select	NP_598328.1:n.1613+331C=