Canonical Allele Identifier: CA799760633
Gene: SNCA HGNC NCBI

Linked Data

dbSNP Id: rs777296100

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89725318_89725319insTAA , CM000666.2:g.89725318_89725319insTAA GRCh38
NC_000004.11:g.90646469_90646470insTAA , CM000666.1:g.90646469_90646470insTAA GRCh37
NC_000004.10:g.90865492_90865493insTAA NCBI36
NG_011851.1:g.117978_117979insTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000394991.8:c.*1309_*1310insTTA MANE Select ENSP00000378442.4:n.*1309_*1310insTTA
ENST00000673718.1:c.*1309_*1310insTTA ENSP00000500990.1:n.*1309_*1310insTTA
ENST00000673766.1:n.1987_1988insTTA
ENST00000673902.1:c.390+3875_390+3876insTTA ENSP00000501102.1:n.390+3875_390+3876insTTA
ENST00000336904.7:c.*1309_*1310insTTA ENSP00000338345.3:n.*1309_*1310insTTA
ENST00000394989.6:c.*1309_*1310insTTA ENSP00000378440.2:n.*1309_*1310insTTA
ENST00000420646.6:c.*1309_*1310insTTA ENSP00000396241.2:n.*1309_*1310insTTA
ENST00000618500.4:c.*1309_*1310insTTA ENSP00000484044.1:n.*1309_*1310insTTA
NM_000345.3:c.*1309_*1310insTTA NP_000336.1:n.*1309_*1310insTTA
NM_001146054.1:c.*1309_*1310insTTA NP_001139526.1:n.*1309_*1310insTTA
NM_001146055.1:c.*1309_*1310insTTA NP_001139527.1:n.*1309_*1310insTTA
NM_007308.2:c.*1309_*1310insTTA NP_009292.1:n.*1309_*1310insTTA
NM_000345.4:c.*1309_*1310insTTA MANE Select NP_000336.1:n.*1309_*1310insTTA
NM_001146054.2:c.*1309_*1310insTTA NP_001139526.1:n.*1309_*1310insTTA
NM_001146055.2:c.*1309_*1310insTTA NP_001139527.1:n.*1309_*1310insTTA
NM_001375285.1:c.*1309_*1310insTTA NP_001362214.1:n.*1309_*1310insTTA
NM_001375286.1:c.*1309_*1310insTTA NP_001362215.1:n.*1309_*1310insTTA
NM_001375287.1:c.*1309_*1310insTTA NP_001362216.1:n.*1309_*1310insTTA
NM_001375288.1:c.*1309_*1310insTTA NP_001362217.1:n.*1309_*1310insTTA
NM_001375290.1:c.*1309_*1310insTTA NP_001362219.1:n.*1309_*1310insTTA
NR_164674.1:n.1277-5_1277-4insTTA
NR_164675.1:n.1424-5_1424-4insTTA
NR_164676.1:n.2030_2031insTTA
NM_007308.3:c.*1309_*1310insTTA NP_009292.1:n.*1309_*1310insTTA