Canonical Allele Identifier: CA799760796
Gene: SNCA HGNC NCBI

Linked Data

dbSNP Id: rs1461262743

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89725350_89725351del , CM000666.2:g.89725350_89725351del GRCh38
NC_000004.11:g.90646501_90646502del , CM000666.1:g.90646501_90646502del GRCh37
NC_000004.10:g.90865524_90865525del NCBI36
NG_011851.1:g.117949_117950del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394991.8:c.*1280_*1281del MANE Select ENSP00000378442.4:n.*1280_*1281del
ENST00000673718.1:c.*1280_*1281del ENSP00000500990.1:n.*1280_*1281del
ENST00000673766.1:n.1958_1959del
ENST00000673902.1:c.390+3846_390+3847del ENSP00000501102.1:n.390+3846_390+3847del
ENST00000674129.1:c.*1280_*1281del ENSP00000501269.1:n.*1280_*1281del
ENST00000336904.7:c.*1280_*1281del ENSP00000338345.3:n.*1280_*1281del
ENST00000394989.6:c.*1280_*1281del ENSP00000378440.2:n.*1280_*1281del
ENST00000420646.6:c.*1280_*1281del ENSP00000396241.2:n.*1280_*1281del
ENST00000618500.4:c.*1280_*1281del ENSP00000484044.1:n.*1280_*1281del
NM_000345.3:c.*1280_*1281del NP_000336.1:n.*1280_*1281del
NM_001146054.1:c.*1280_*1281del NP_001139526.1:n.*1280_*1281del
NM_001146055.1:c.*1280_*1281del NP_001139527.1:n.*1280_*1281del
NM_007308.2:c.*1280_*1281del NP_009292.1:n.*1280_*1281del
NM_000345.4:c.*1280_*1281del MANE Select NP_000336.1:n.*1280_*1281del
NM_001146054.2:c.*1280_*1281del NP_001139526.1:n.*1280_*1281del
NM_001146055.2:c.*1280_*1281del NP_001139527.1:n.*1280_*1281del
NM_001375285.1:c.*1280_*1281del NP_001362214.1:n.*1280_*1281del
NM_001375286.1:c.*1280_*1281del NP_001362215.1:n.*1280_*1281del
NM_001375287.1:c.*1280_*1281del NP_001362216.1:n.*1280_*1281del
NM_001375288.1:c.*1280_*1281del NP_001362217.1:n.*1280_*1281del
NM_001375290.1:c.*1280_*1281del NP_001362219.1:n.*1280_*1281del
NR_164674.1:n.1277-34_1277-33del
NR_164675.1:n.1424-34_1424-33del
NR_164676.1:n.2001_2002del
NM_007308.3:c.*1280_*1281del NP_009292.1:n.*1280_*1281del