Canonical Allele Identifier: CA2427971862

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47576131C= , CM000685.2:g.47576131C=	GRCh38
NC_000023.10:g.47435530C= , CM000685.1:g.47435530C=	GRCh37
NC_000023.9:g.47320474C=	NCBI36
NG_008437.1:g.48727G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295987.13:c.1158G= MANE Select	ENSP00000295987.7:p.Glu386=
ENST00000340666.5:c.1158G=	ENSP00000343206.4:p.Glu386=
ENST00000295987.11:c.1158G=	ENSP00000295987.7:p.Glu386=
ENST00000340666.4:c.1158G=	ENSP00000343206.4:p.Glu386=
NM_006950.3:c.1158G= MANE Select	NP_008881.2:p.Glu386=
NM_133499.2:c.1158G=	NP_598006.1:p.Glu386=