Canonical Allele Identifier: CA2427971887

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47576222C= , CM000685.2:g.47576222C=	GRCh38
NC_000023.10:g.47435621C= , CM000685.1:g.47435621C=	GRCh37
NC_000023.9:g.47320565C=	NCBI36
NG_008437.1:g.48636G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295987.13:c.1067G= MANE Select	ENSP00000295987.7:p.Trp356=
ENST00000340666.5:c.1067G=	ENSP00000343206.4:p.Trp356=
ENST00000295987.11:c.1067G=	ENSP00000295987.7:p.Trp356=
ENST00000340666.4:c.1067G=	ENSP00000343206.4:p.Trp356=
NM_006950.3:c.1067G= MANE Select	NP_008881.2:p.Trp356=
NM_133499.2:c.1067G=	NP_598006.1:p.Trp356=