Canonical Allele Identifier: CA2580101026

Gene: SYN1

Linked Data

• ClinVar Variation Id: 1710320
• ClinVar RCV Id: RCV002291327

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574578dup , CM000685.2:g.47574578dup	GRCh38
NC_000023.10:g.47433977dup , CM000685.1:g.47433977dup	GRCh37
NC_000023.9:g.47318921dup	NCBI36
NG_008437.1:g.50280dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1406dup MANE Select	ENSP00000295987.7:p.Pro470AlafsTer?
ENST00000340666.5:c.1406dup	ENSP00000343206.4:p.Pro470AlafsTer?
ENST00000640721.1:c.70+110dup	ENSP00000492857.1:n.70+110dup
ENST00000295987.11:c.1406dup	ENSP00000295987.7:p.Pro470AlafsTer?
ENST00000340666.4:c.1406dup	ENSP00000343206.4:p.Pro470AlafsTer?
NM_006950.3:c.1406dup MANE Select	NP_008881.2:p.Pro470AlafsTer?
NM_133499.2:c.1406dup	NP_598006.1:p.Pro470AlafsTer?