Canonical Allele Identifier: CA1346036783

Gene: SYN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12167171G= , CM000665.2:g.12167171G=	GRCh38
NC_000003.11:g.12208671G= , CM000665.1:g.12208671G=	GRCh37
NC_000003.10:g.12183671G=	NCBI36
NG_011728.2:g.167784G=

Transcript Alleles

HGVS	Amino-acid Change
NM_133625.6:c.981-63G= MANE Select	NP_598328.1:n.981-63G=
ENST00000621198.5:c.981-63G= MANE Select	ENSP00000480050.1:n.981-63G=
NM_003178.5:c.981-63G=	NP_003169.2:n.981-63G=
NM_003178.6:c.981-63G=	NP_003169.2:n.981-63G=
NM_133625.4:c.981-63G=	NP_598328.1:n.981-63G=
NM_133625.5:c.981-63G=	NP_598328.1:n.981-63G=
ENST00000425297.2:c.208-63G=
ENST00000439861.5:n.600-63G=
ENST00000447752.2:n.430-63G=
ENST00000620175.4:c.981-63G=	ENSP00000484916.1:n.981-63G=
ENST00000621198.4:c.981-63G=	ENSP00000480050.1:n.981-63G=
XM_006713311.2:c.981-63G=	XP_006713374.1:n.981-63G=
XM_006713311.3:c.981-63G=	XP_006713374.1:n.981-63G=
XM_006713312.2:c.498-63G=	XP_006713375.1:n.498-63G=
XM_006713312.4:c.498-63G=	XP_006713375.1:n.498-63G=
XM_006713313.2:c.210-63G=	XP_006713376.1:n.210-63G=
XM_017007087.1:c.309-63G=	XP_016862576.1:n.309-63G=
XR_001740240.1:n.1335-63G=