Canonical Allele Identifier: CA2820775701

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47573261A>C , CM000685.2:g.47573261A>C	GRCh38
NC_000023.10:g.47432660A>C , CM000685.1:g.47432660A>C	GRCh37
NC_000023.9:g.47317604A>C	NCBI36
NG_008437.1:g.51597T>G
NG_016339.1:g.17145A>C
NG_016339.2:g.17145A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1983-262T>G MANE Select	ENSP00000295987.7:n.1983-262T>G
ENST00000340666.5:c.1983-300T>G	ENSP00000343206.4:n.1983-300T>G
ENST00000640721.1:c.71-300T>G	ENSP00000492857.1:n.71-300T>G
ENST00000295987.11:c.1983-262T>G	ENSP00000295987.7:n.1983-262T>G
ENST00000340666.4:c.1983-300T>G	ENSP00000343206.4:n.1983-300T>G
NM_006950.3:c.1983-262T>G MANE Select	NP_008881.2:n.1983-262T>G
NM_133499.2:c.1983-300T>G	NP_598006.1:n.1983-300T>G