Canonical Allele Identifier: CA2427970894

Gene: SYN1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47573257G= , CM000685.2:g.47573257G=	GRCh38
NC_000023.10:g.47432656G= , CM000685.1:g.47432656G=	GRCh37
NC_000023.9:g.47317600G=	NCBI36
NG_008437.1:g.51601C=
NG_016339.1:g.17141G=
NG_016339.2:g.17141G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295987.13:c.1983-258C= MANE Select	ENSP00000295987.7:n.1983-258C=
ENST00000340666.5:c.1983-296C=	ENSP00000343206.4:n.1983-296C=
ENST00000640721.1:c.71-296C=	ENSP00000492857.1:n.71-296C=
ENST00000295987.11:c.1983-258C=	ENSP00000295987.7:n.1983-258C=
ENST00000340666.4:c.1983-296C=	ENSP00000343206.4:n.1983-296C=
NM_006950.3:c.1983-258C= MANE Select	NP_008881.2:n.1983-258C=
NM_133499.2:c.1983-296C=	NP_598006.1:n.1983-296C=