Canonical Allele Identifier: CA1475333177

Gene: SNCA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89716420G= , CM000666.2:g.89716420G=	GRCh38
NC_000004.11:g.90637571G= , CM000666.1:g.90637571G=	GRCh37
NC_000004.10:g.90856594G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673902.1:c.390+12774C=	ENSP00000501102.1:n.390+12774C=
XR_938982.1:n.3490-3406G=
XR_938984.1:n.2890-3406G=
XR_938985.1:n.1922-3406G=
XR_938986.1:n.556-3406G=
XR_938987.1:n.810-3406G=
XR_938988.1:n.676-3406G=
XR_938989.1:n.332-3406G=
XR_938990.1:n.420-3406G=
XR_938991.1:n.435-3406G=
XR_938993.1:n.437-3406G=
XR_938994.1:n.901-3406G=
XR_938995.1:n.735-3406G=
XR_001741765.1:n.2908-3406G=
XR_001741766.1:n.1680-3406G=
XR_938982.2:n.3490-3406G=
XR_938984.2:n.2912-3406G=
XR_938985.2:n.1944-3406G=
XR_938986.2:n.581-3406G=
XR_938987.2:n.870-3406G=
XR_938989.2:n.354-3406G=