Canonical Allele Identifier: CA553252522
Gene: SNCA HGNC NCBI

Linked Data

dbSNP Id: rs1724791067

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89725336_89725347del , CM000666.2:g.89725336_89725347del GRCh38
NC_000004.11:g.90646487_90646498del , CM000666.1:g.90646487_90646498del GRCh37
NC_000004.10:g.90865510_90865521del NCBI36
NG_011851.1:g.117951_117962del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394991.8:c.*1282_*1293del MANE Select ENSP00000378442.4:n.*1282_*1293del
ENST00000673718.1:c.*1282_*1293del ENSP00000500990.1:n.*1282_*1293del
ENST00000673766.1:n.1960_1971del
ENST00000673902.1:c.390+3848_390+3859del ENSP00000501102.1:n.390+3848_390+3859del
ENST00000336904.7:c.*1282_*1293del ENSP00000338345.3:n.*1282_*1293del
ENST00000394989.6:c.*1282_*1293del ENSP00000378440.2:n.*1282_*1293del
ENST00000420646.6:c.*1282_*1293del ENSP00000396241.2:n.*1282_*1293del
ENST00000618500.4:c.*1282_*1293del ENSP00000484044.1:n.*1282_*1293del
NM_000345.3:c.*1282_*1293del NP_000336.1:n.*1282_*1293del
NM_001146054.1:c.*1282_*1293del NP_001139526.1:n.*1282_*1293del
NM_001146055.1:c.*1282_*1293del NP_001139527.1:n.*1282_*1293del
NM_007308.2:c.*1282_*1293del NP_009292.1:n.*1282_*1293del
NM_000345.4:c.*1282_*1293del MANE Select NP_000336.1:n.*1282_*1293del
NM_001146054.2:c.*1282_*1293del NP_001139526.1:n.*1282_*1293del
NM_001146055.2:c.*1282_*1293del NP_001139527.1:n.*1282_*1293del
NM_001375285.1:c.*1282_*1293del NP_001362214.1:n.*1282_*1293del
NM_001375286.1:c.*1282_*1293del NP_001362215.1:n.*1282_*1293del
NM_001375287.1:c.*1282_*1293del NP_001362216.1:n.*1282_*1293del
NM_001375288.1:c.*1282_*1293del NP_001362217.1:n.*1282_*1293del
NM_001375290.1:c.*1282_*1293del NP_001362219.1:n.*1282_*1293del
NR_164674.1:n.1277-32_1277-21del
NR_164675.1:n.1424-32_1424-21del
NR_164676.1:n.2003_2014del
NM_007308.3:c.*1282_*1293del NP_009292.1:n.*1282_*1293del