Canonical Allele Identifier: CA2427970807

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47572959G= , CM000685.2:g.47572959G=	GRCh38
NC_000023.10:g.47432358G= , CM000685.1:g.47432358G=	GRCh37
NC_000023.9:g.47317302G=	NCBI36
NG_008437.1:g.51899C=
NG_016339.1:g.16843G=
NG_016339.2:g.16843G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295987.13:c.2023C= MANE Select	ENSP00000295987.7:p.Pro675=
ENST00000340666.5:c.1985C=	ENSP00000343206.4:p.Ala662=
ENST00000640721.1:c.73C=	ENSP00000492857.1:p.Pro25=
ENST00000295987.11:c.2023C=	ENSP00000295987.7:p.Pro675=
ENST00000340666.4:c.1985C=	ENSP00000343206.4:p.Ala662=
NM_006950.3:c.2023C= MANE Select	NP_008881.2:p.Pro675=
NM_133499.2:c.1985C=	NP_598006.1:p.Ala662=