Canonical Allele Identifier: CA2701931307

Gene: SYN2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12022931_12022933del , CM000665.2:g.12022931_12022933del	GRCh38
NC_000003.11:g.12064431_12064433del , CM000665.1:g.12064431_12064433del	GRCh37
NC_000003.10:g.12039431_12039433del	NCBI36
NG_011728.2:g.23544_23546del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.377+18003_377+18005del MANE Select	ENSP00000480050.1:n.377+18003_377+18005del
ENST00000620175.4:c.377+18003_377+18005del	ENSP00000484916.1:n.377+18003_377+18005del
ENST00000621198.4:c.377+18003_377+18005del	ENSP00000480050.1:n.377+18003_377+18005del
NM_003178.5:c.377+18003_377+18005del	NP_003169.2:n.377+18003_377+18005del
NM_133625.4:c.377+18003_377+18005del	NP_598328.1:n.377+18003_377+18005del
XM_006713311.2:c.377+18003_377+18005del	XP_006713374.1:n.377+18003_377+18005del
XM_006713311.3:c.377+18003_377+18005del	XP_006713374.1:n.377+18003_377+18005del
XR_001740240.1:n.563+18003_563+18005del
NM_133625.5:c.377+18003_377+18005del	NP_598328.1:n.377+18003_377+18005del
NM_133625.6:c.377+18003_377+18005del MANE Select	NP_598328.1:n.377+18003_377+18005del
NM_003178.6:c.377+18003_377+18005del	NP_003169.2:n.377+18003_377+18005del