Canonical Allele Identifier: CA2427970899

Gene: SYN1

Linked Data

• dbSNP Id: rs2057765809

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47573272_47573273insTTGCC , CM000685.2:g.47573272_47573273insTTGCC	GRCh38
NC_000023.10:g.47432671_47432672insTTGCC , CM000685.1:g.47432671_47432672insTTGCC	GRCh37
NC_000023.9:g.47317615_47317616insTTGCC	NCBI36
NG_008437.1:g.51586_51587insGCAAG
NG_016339.1:g.17156_17157insTTGCC
NG_016339.2:g.17156_17157insTTGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1983-273_1983-272insGCAAG MANE Select	ENSP00000295987.7:n.1983-273_1983-272insGCAAG
ENST00000340666.5:c.1983-311_1983-310insGCAAG	ENSP00000343206.4:n.1983-311_1983-310insGCAAG
ENST00000640721.1:c.71-311_71-310insGCAAG	ENSP00000492857.1:n.71-311_71-310insGCAAG
ENST00000295987.11:c.1983-273_1983-272insGCAAG	ENSP00000295987.7:n.1983-273_1983-272insGCAAG
ENST00000340666.4:c.1983-311_1983-310insGCAAG	ENSP00000343206.4:n.1983-311_1983-310insGCAAG
NM_006950.3:c.1983-273_1983-272insGCAAG MANE Select	NP_008881.2:n.1983-273_1983-272insGCAAG
NM_133499.2:c.1983-311_1983-310insGCAAG	NP_598006.1:n.1983-311_1983-310insGCAAG