Canonical Allele Identifier: CA69988975

Gene: SYN2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12045605_12045609del , CM000665.2:g.12045605_12045609del	GRCh38
NC_000003.11:g.12087105_12087109del , CM000665.1:g.12087105_12087109del	GRCh37
NC_000003.10:g.12062105_12062109del	NCBI36
NG_011728.2:g.46218_46222del

Transcript Alleles

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