Canonical Allele Identifier: CA2427971175

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574059T= , CM000685.2:g.47574059T=	GRCh38
NC_000023.10:g.47433458T= , CM000685.1:g.47433458T=	GRCh37
NC_000023.9:g.47318402T=	NCBI36
NG_008437.1:g.50799A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1925A= MANE Select	ENSP00000295987.7:p.Gln642=
ENST00000340666.5:c.1925A=	ENSP00000343206.4:p.Gln642=
ENST00000640721.1:c.70+629A=	ENSP00000492857.1:n.70+629A=
ENST00000295987.11:c.1925A=	ENSP00000295987.7:p.Gln642=
ENST00000340666.4:c.1925A=	ENSP00000343206.4:p.Gln642=
NM_006950.3:c.1925A= MANE Select	NP_008881.2:p.Gln642=
NM_133499.2:c.1925A=	NP_598006.1:p.Gln642=