Canonical Allele Identifier: CA2427971318

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47574511C= , CM000685.2:g.47574511C=	GRCh38
NC_000023.10:g.47433910C= , CM000685.1:g.47433910C=	GRCh37
NC_000023.9:g.47318854C=	NCBI36
NG_008437.1:g.50347G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1473G= MANE Select	ENSP00000295987.7:p.Gln491=
ENST00000340666.5:c.1473G=	ENSP00000343206.4:p.Gln491=
ENST00000640721.1:c.70+177G=	ENSP00000492857.1:n.70+177G=
ENST00000295987.11:c.1473G=	ENSP00000295987.7:p.Gln491=
ENST00000340666.4:c.1473G=	ENSP00000343206.4:p.Gln491=
NM_006950.3:c.1473G= MANE Select	NP_008881.2:p.Gln491=
NM_133499.2:c.1473G=	NP_598006.1:p.Gln491=