Canonical Allele Identifier: CA2820776441

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47588446G>A , CM000685.2:g.47588446G>A	GRCh38
NC_000023.10:g.47447845G>A , CM000685.1:g.47447845G>A	GRCh37
NC_000023.9:g.47332789G>A	NCBI36
NG_008437.1:g.36412C>T
NG_012533.1:g.11156G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.775-10945C>T MANE Select	ENSP00000295987.7:n.775-10945C>T
ENST00000340666.5:c.775-10945C>T	ENSP00000343206.4:n.775-10945C>T
ENST00000295987.11:c.775-10945C>T	ENSP00000295987.7:n.775-10945C>T
ENST00000340666.4:c.775-10945C>T	ENSP00000343206.4:n.775-10945C>T
NM_006950.3:c.775-10945C>T MANE Select	NP_008881.2:n.775-10945C>T
NM_133499.2:c.775-10945C>T	NP_598006.1:n.775-10945C>T