Canonical Allele Identifier: CA2840723080

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574822dup , CM000685.2:g.47574822dup	GRCh38
NC_000023.10:g.47434221dup , CM000685.1:g.47434221dup	GRCh37
NC_000023.9:g.47319165dup	NCBI36
NG_008437.1:g.50037dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1306-46dup MANE Select	ENSP00000295987.7:n.1306-46dup
ENST00000340666.5:c.1306-46dup	ENSP00000343206.4:n.1306-46dup
ENST00000295987.11:c.1306-46dup	ENSP00000295987.7:n.1306-46dup
ENST00000340666.4:c.1306-46dup	ENSP00000343206.4:n.1306-46dup
NM_006950.3:c.1306-46dup MANE Select	NP_008881.2:n.1306-46dup
NM_133499.2:c.1306-46dup	NP_598006.1:n.1306-46dup