Canonical Allele Identifier: CA2427970808

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47572973A= , CM000685.2:g.47572973A=	GRCh38
NC_000023.10:g.47432372A= , CM000685.1:g.47432372A=	GRCh37
NC_000023.9:g.47317316A=	NCBI36
NG_008437.1:g.51885T=
NG_016339.1:g.16857A=
NG_016339.2:g.16857A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.2009T= MANE Select	ENSP00000295987.7:p.Phe670=
ENST00000340666.5:c.1983-12T=	ENSP00000343206.4:n.1983-12T=
ENST00000640721.1:c.71-12T=	ENSP00000492857.1:n.71-12T=
ENST00000295987.11:c.2009T=	ENSP00000295987.7:p.Phe670=
ENST00000340666.4:c.1983-12T=	ENSP00000343206.4:n.1983-12T=
NM_006950.3:c.2009T= MANE Select	NP_008881.2:p.Phe670=
NM_133499.2:c.1983-12T=	NP_598006.1:n.1983-12T=