Canonical Allele Identifier: CA257069
Gene: SNCA HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14008
ClinVar RCV Id: RCV000015045
dbSNP Id: rs104893878

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89835580C>G , CM000666.2:g.89835580C>G GRCh38
NC_000004.11:g.90756731C>G , CM000666.1:g.90756731C>G GRCh37
NC_000004.10:g.90975754C>G NCBI36
NG_011851.1:g.7717G>C

Transcript Alleles

HGVS Amino-acid change
NM_000345.3:c.88G>C VV NP_000336.1:p.Ala30Pro
NM_001146054.1:c.88G>C VV NP_001139526.1:p.Ala30Pro
NM_001146055.1:c.88G>C VV NP_001139527.1:p.Ala30Pro
NM_007308.2:c.88G>C VV NP_009292.1:p.Ala30Pro
XM_011532203.1:c.88G>C XP_011530505.1:p.Ala30Pro
XM_011532204.1:c.88G>C XP_011530506.1:p.Ala30Pro
XM_011532205.1:c.88G>C XP_011530507.1:p.Ala30Pro
XM_011532206.1:c.88G>C XP_011530508.1:p.Ala30Pro
XM_011532207.1:c.88G>C XP_011530509.1:p.Ala30Pro
XM_011532208.1:c.88G>C XP_011530510.1:p.Ala30Pro
XM_011532204.3:c.88G>C
XM_011532205.2:c.88G>C
XM_011532208.2:c.88G>C
XM_017008562.1:c.88G>C XP_016864051.1:p.Ala30Pro
XM_017008563.1:c.88G>C XP_016864052.1:p.Ala30Pro
ENST00000336904.7:c.88G>C ENSP00000338345.3:p.Ala30Pro
ENST00000345009.8:c.88G>C ENSP00000343683.4:p.Ala30Pro
ENST00000394986.5:c.88G>C ENSP00000378437.1:p.Ala30Pro
ENST00000394989.6:c.88G>C ENSP00000378440.2:p.Ala30Pro
ENST00000394991.7:c.88G>C ENSP00000378442.3:p.Ala30Pro
ENST00000420646.6:c.88G>C ENSP00000396241.2:p.Ala30Pro
ENST00000502987.5:c.88G>C ENSP00000426034.1:p.Ala30Pro
ENST00000505199.5:c.88G>C ENSP00000421485.1:p.Ala30Pro
ENST00000506244.5:c.88G>C ENSP00000422238.1:p.Ala30Pro
ENST00000506691.1:c.88G>C ENSP00000423445.1:p.Ala30Pro
ENST00000508895.5:c.88G>C ENSP00000426955.1:p.Ala30Pro
ENST00000611107.1:n.88G>C ENSP00000479604.1:p.Ala30Pro
ENST00000618500.4:c.88G>C ENSP00000484044.1:p.Ala30Pro