Canonical Allele Identifier: CA2427971168

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574043G= , CM000685.2:g.47574043G=	GRCh38
NC_000023.10:g.47433442G= , CM000685.1:g.47433442G=	GRCh37
NC_000023.9:g.47318386G=	NCBI36
NG_008437.1:g.50815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1941C= MANE Select	ENSP00000295987.7:p.Pro647=
ENST00000340666.5:c.1941C=	ENSP00000343206.4:p.Pro647=
ENST00000640721.1:c.70+645C=	ENSP00000492857.1:n.70+645C=
ENST00000295987.11:c.1941C=	ENSP00000295987.7:p.Pro647=
ENST00000340666.4:c.1941C=	ENSP00000343206.4:p.Pro647=
NM_006950.3:c.1941C= MANE Select	NP_008881.2:p.Pro647=
NM_133499.2:c.1941C=	NP_598006.1:p.Pro647=