Canonical Allele Identifier: CA69951922

Gene: SYN2

Linked Data

• dbSNP Id: rs72580747
• MyVariant Identifiers: chr3:g.12064432_12064433insACA (hg19) ; chr3:g.12022932_12022933insACA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12022934_12022935insAAC , CM000665.2:g.12022934_12022935insAAC	GRCh38
NC_000003.11:g.12064434_12064435insAAC , CM000665.1:g.12064434_12064435insAAC	GRCh37
NC_000003.10:g.12039434_12039435insAAC	NCBI36
NG_011728.2:g.23547_23548insAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.377+18006_377+18007insAAC MANE Select	ENSP00000480050.1:n.377+18006_377+18007insAAC
ENST00000620175.4:c.377+18006_377+18007insAAC	ENSP00000484916.1:n.377+18006_377+18007insAAC
ENST00000621198.4:c.377+18006_377+18007insAAC	ENSP00000480050.1:n.377+18006_377+18007insAAC
NM_003178.5:c.377+18006_377+18007insAAC	NP_003169.2:n.377+18006_377+18007insAAC
NM_133625.4:c.377+18006_377+18007insAAC	NP_598328.1:n.377+18006_377+18007insAAC
XM_006713311.2:c.377+18006_377+18007insAAC	XP_006713374.1:n.377+18006_377+18007insAAC
XM_006713311.3:c.377+18006_377+18007insAAC	XP_006713374.1:n.377+18006_377+18007insAAC
XR_001740240.1:n.563+18006_563+18007insAAC
NM_133625.5:c.377+18006_377+18007insAAC	NP_598328.1:n.377+18006_377+18007insAAC
NM_133625.6:c.377+18006_377+18007insAAC MANE Select	NP_598328.1:n.377+18006_377+18007insAAC
NM_003178.6:c.377+18006_377+18007insAAC	NP_003169.2:n.377+18006_377+18007insAAC