Canonical Allele Identifier: CA2427971889

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47576226G= , CM000685.2:g.47576226G=	GRCh38
NC_000023.10:g.47435625G= , CM000685.1:g.47435625G=	GRCh37
NC_000023.9:g.47320569G=	NCBI36
NG_008437.1:g.48632C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295987.13:c.1063C= MANE Select	ENSP00000295987.7:p.Leu355=
ENST00000340666.5:c.1063C=	ENSP00000343206.4:p.Leu355=
ENST00000295987.11:c.1063C=	ENSP00000295987.7:p.Leu355=
ENST00000340666.4:c.1063C=	ENSP00000343206.4:p.Leu355=
NM_006950.3:c.1063C= MANE Select	NP_008881.2:p.Leu355=
NM_133499.2:c.1063C=	NP_598006.1:p.Leu355=