Canonical Allele Identifier: CA11397647

Gene: SYN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12182651T>C , CM000665.2:g.12182651T>C	GRCh38
NC_000003.11:g.12224151T>C , CM000665.1:g.12224151T>C	GRCh37
NC_000003.10:g.12199151T>C	NCBI36
NG_011728.2:g.183264T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.1309-661T>C MANE Select	ENSP00000480050.1:n.1309-661T>C
ENST00000425297.2:c.536-661T>C
ENST00000439861.5:n.928-661T>C
ENST00000620175.4:c.1309-661T>C	ENSP00000484916.1:n.1309-661T>C
ENST00000621198.4:c.1309-661T>C	ENSP00000480050.1:n.1309-661T>C
NM_003178.5:c.1309-661T>C	NP_003169.2:n.1309-661T>C
NM_133625.4:c.1309-661T>C	NP_598328.1:n.1309-661T>C
XM_006713312.2:c.826-661T>C	XP_006713375.1:n.826-661T>C
XM_006713313.2:c.538-661T>C	XP_006713376.1:n.538-661T>C
XM_006713312.4:c.826-661T>C	XP_006713375.1:n.826-661T>C
XM_017007087.1:c.637-661T>C	XP_016862576.1:n.637-661T>C
XR_001740240.1:n.1663-661T>C
NM_133625.5:c.1309-661T>C	NP_598328.1:n.1309-661T>C
NM_133625.6:c.1309-661T>C MANE Select	NP_598328.1:n.1309-661T>C
NM_003178.6:c.1309-661T>C	NP_003169.2:n.1309-661T>C