Canonical Allele Identifier: CA1346039269

Gene: SYN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12187927T= , CM000665.2:g.12187927T=	GRCh38
NC_000003.11:g.12229427T= , CM000665.1:g.12229427T=	GRCh37
NC_000003.10:g.12204427T=	NCBI36
NG_011728.2:g.188540T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.1613+315T= MANE Select	ENSP00000480050.1:n.1613+315T=
ENST00000439861.5:n.1232+315T=
ENST00000621198.4:c.1613+315T=	ENSP00000480050.1:n.1613+315T=
NM_133625.4:c.1613+315T=	NP_598328.1:n.1613+315T=
XM_006713312.2:c.1130+315T=	XP_006713375.1:n.1130+315T=
XM_006713313.2:c.842+315T=	XP_006713376.1:n.842+315T=
XM_006713312.4:c.1130+315T=	XP_006713375.1:n.1130+315T=
XM_017007087.1:c.941+315T=	XP_016862576.1:n.941+315T=
NM_133625.5:c.1613+315T=	NP_598328.1:n.1613+315T=
NM_133625.6:c.1613+315T= MANE Select	NP_598328.1:n.1613+315T=