Canonical Allele Identifier: CA2427971359

Gene: SYN1

Linked Data

• dbSNP Id: rs1268259768

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574633G>C , CM000685.2:g.47574633G>C	GRCh38
NC_000023.10:g.47434032G>C , CM000685.1:g.47434032G>C	GRCh37
NC_000023.9:g.47318976G>C	NCBI36
NG_008437.1:g.50225C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1394-43C>G MANE Select	ENSP00000295987.7:n.1394-43C>G
ENST00000340666.5:c.1394-43C>G	ENSP00000343206.4:n.1394-43C>G
ENST00000640721.1:c.70+55C>G	ENSP00000492857.1:n.70+55C>G
ENST00000295987.11:c.1394-43C>G	ENSP00000295987.7:n.1394-43C>G
ENST00000340666.4:c.1394-43C>G	ENSP00000343206.4:n.1394-43C>G
NM_006950.3:c.1394-43C>G MANE Select	NP_008881.2:n.1394-43C>G
NM_133499.2:c.1394-43C>G	NP_598006.1:n.1394-43C>G