Canonical Allele Identifier: CA1475333170

Gene: SNCA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89716399G= , CM000666.2:g.89716399G=	GRCh38
NC_000004.11:g.90637550G= , CM000666.1:g.90637550G=	GRCh37
NC_000004.10:g.90856573G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000673902.1:c.390+12795C=	ENSP00000501102.1:n.390+12795C=
XR_938982.1:n.3490-3427G=
XR_938984.1:n.2890-3427G=
XR_938985.1:n.1922-3427G=
XR_938986.1:n.556-3427G=
XR_938987.1:n.810-3427G=
XR_938988.1:n.676-3427G=
XR_938989.1:n.332-3427G=
XR_938990.1:n.420-3427G=
XR_938991.1:n.435-3427G=
XR_938993.1:n.437-3427G=
XR_938994.1:n.901-3427G=
XR_938995.1:n.735-3427G=
XR_001741765.1:n.2908-3427G=
XR_001741766.1:n.1680-3427G=
XR_938982.2:n.3490-3427G=
XR_938984.2:n.2912-3427G=
XR_938985.2:n.1944-3427G=
XR_938986.2:n.581-3427G=
XR_938987.2:n.870-3427G=
XR_938989.2:n.354-3427G=