Canonical Allele Identifier: CA2427970784

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47572870G= , CM000685.2:g.47572870G=	GRCh38
NC_000023.10:g.47432269G= , CM000685.1:g.47432269G=	GRCh37
NC_000023.9:g.47317213G=	NCBI36
NG_008437.1:g.51988C=
NG_016339.1:g.16754G=
NG_016339.2:g.16754G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295987.13:c.2112C= MANE Select	ENSP00000295987.7:p.Ser704=
ENST00000340666.5:c.*64C=	ENSP00000343206.4:n.*64C=
ENST00000640721.1:c.162C=	ENSP00000492857.1:p.Ser54=
ENST00000295987.11:c.2112C=	ENSP00000295987.7:p.Ser704=
ENST00000340666.4:c.*64C=	ENSP00000343206.4:n.*64C=
NM_006950.3:c.2112C= MANE Select	NP_008881.2:p.Ser704=
NM_133499.2:c.*64C=	NP_598006.1:n.*64C=