Canonical Allele Identifier: CA69988973

Gene: SYN2

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12045605_12045609dup , CM000665.2:g.12045605_12045609dup	GRCh38
NC_000003.11:g.12087105_12087109dup , CM000665.1:g.12087105_12087109dup	GRCh37
NC_000003.10:g.12062105_12062109dup	NCBI36
NG_011728.2:g.46218_46222dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.377+40677_377+40681dup MANE Select	ENSP00000480050.1:n.377+40677_377+40681dup
ENST00000620175.4:c.377+40677_377+40681dup	ENSP00000484916.1:n.377+40677_377+40681dup
ENST00000621198.4:c.377+40677_377+40681dup	ENSP00000480050.1:n.377+40677_377+40681dup
NM_003178.5:c.377+40677_377+40681dup	NP_003169.2:n.377+40677_377+40681dup
NM_133625.4:c.377+40677_377+40681dup	NP_598328.1:n.377+40677_377+40681dup
XM_006713311.2:c.377+40677_377+40681dup	XP_006713374.1:n.377+40677_377+40681dup
XM_006713311.3:c.377+40677_377+40681dup	XP_006713374.1:n.377+40677_377+40681dup
XR_001740240.1:n.563+40677_563+40681dup
NM_133625.5:c.377+40677_377+40681dup	NP_598328.1:n.377+40677_377+40681dup
NM_133625.6:c.377+40677_377+40681dup MANE Select	NP_598328.1:n.377+40677_377+40681dup
NM_003178.6:c.377+40677_377+40681dup	NP_003169.2:n.377+40677_377+40681dup