Canonical Allele Identifier: CA2567334600

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47573003G>T , CM000685.2:g.47573003G>T	GRCh38
NC_000023.10:g.47432402G>T , CM000685.1:g.47432402G>T	GRCh37
NC_000023.9:g.47317346G>T	NCBI36
NG_008437.1:g.51855C>A
NG_016339.1:g.16887G>T
NG_016339.2:g.16887G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1983-4C>A MANE Select	ENSP00000295987.7:n.1983-4C>A
ENST00000340666.5:c.1983-42C>A	ENSP00000343206.4:n.1983-42C>A
ENST00000640721.1:c.71-42C>A	ENSP00000492857.1:n.71-42C>A
ENST00000295987.11:c.1983-4C>A	ENSP00000295987.7:n.1983-4C>A
ENST00000340666.4:c.1983-42C>A	ENSP00000343206.4:n.1983-42C>A
NM_006950.3:c.1983-4C>A MANE Select	NP_008881.2:n.1983-4C>A
NM_133499.2:c.1983-42C>A	NP_598006.1:n.1983-42C>A