Canonical Allele Identifier: CA101495029

Gene: SNCA

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89704988G>A , CM000666.2:g.89704988G>A	GRCh38
NC_000004.11:g.90626139G>A , CM000666.1:g.90626139G>A	GRCh37
NC_000004.10:g.90845162G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673902.1:c.391-2604C>T	ENSP00000501102.1:n.391-2604C>T
XR_938982.1:n.3489+13583G>A
XR_938984.1:n.2889+13583G>A
XR_938985.1:n.1921+13583G>A
XR_938986.1:n.555+13583G>A
XR_938987.1:n.809+13583G>A
XR_938988.1:n.675+13583G>A
XR_938989.1:n.331+13583G>A
XR_938990.1:n.419+13583G>A
XR_938991.1:n.435-14838G>A
XR_938993.1:n.436+13583G>A
XR_938994.1:n.900+13583G>A
XR_938995.1:n.734+13583G>A
XR_001741765.1:n.2907+13583G>A
XR_001741766.1:n.1679+13583G>A
XR_938982.2:n.3489+13583G>A
XR_938984.2:n.2911+13583G>A
XR_938985.2:n.1943+13583G>A
XR_938986.2:n.580+13583G>A
XR_938987.2:n.869+13583G>A
XR_938989.2:n.353+13583G>A