Canonical Allele Identifier: CA916835805

Gene: SYN2

Linked Data

• dbSNP Id: rs1559435807

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12139904dup , CM000665.2:g.12139904dup	GRCh38
NC_000003.11:g.12181404dup , CM000665.1:g.12181404dup	GRCh37
NC_000003.10:g.12156404dup	NCBI36
NG_011728.2:g.140517dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.378-747dup MANE Select	ENSP00000480050.1:n.378-747dup
ENST00000424884.1:n.127-747dup
ENST00000620175.4:c.378-747dup	ENSP00000484916.1:n.378-747dup
ENST00000621198.4:c.378-747dup	ENSP00000480050.1:n.378-747dup
NM_003178.5:c.378-747dup	NP_003169.2:n.378-747dup
NM_133625.4:c.378-747dup	NP_598328.1:n.378-747dup
XM_006713311.2:c.378-747dup	XP_006713374.1:n.378-747dup
XM_006713311.3:c.378-747dup	XP_006713374.1:n.378-747dup
XR_001740240.1:n.564-747dup
NM_133625.5:c.378-747dup	NP_598328.1:n.378-747dup
NM_133625.6:c.378-747dup MANE Select	NP_598328.1:n.378-747dup
NM_003178.6:c.378-747dup	NP_003169.2:n.378-747dup