Canonical Allele Identifier: CA2427970804

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47572954G= , CM000685.2:g.47572954G=	GRCh38
NC_000023.10:g.47432353G= , CM000685.1:g.47432353G=	GRCh37
NC_000023.9:g.47317297G=	NCBI36
NG_008437.1:g.51904C=
NG_016339.1:g.16838G=
NG_016339.2:g.16838G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.2028C= MANE Select	ENSP00000295987.7:p.Ala676=
ENST00000340666.5:c.1990C=	ENSP00000343206.4:p.Pro664=
ENST00000640721.1:c.78C=	ENSP00000492857.1:p.Ala26=
ENST00000295987.11:c.2028C=	ENSP00000295987.7:p.Ala676=
ENST00000340666.4:c.1990C=	ENSP00000343206.4:p.Pro664=
NM_006950.3:c.2028C= MANE Select	NP_008881.2:p.Ala676=
NM_133499.2:c.1990C=	NP_598006.1:p.Pro664=