Canonical Allele Identifier: CA799760670
Gene: SNCA HGNC NCBI

Linked Data

dbSNP Id: rs1491402669

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89725321_89725322insCAA , CM000666.2:g.89725321_89725322insCAA GRCh38
NC_000004.11:g.90646472_90646473insCAA , CM000666.1:g.90646472_90646473insCAA GRCh37
NC_000004.10:g.90865495_90865496insCAA NCBI36
NG_011851.1:g.117977_117978insGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394991.8:c.*1308_*1309insGTT MANE Select ENSP00000378442.4:n.*1308_*1309insGTT
ENST00000673718.1:c.*1308_*1309insGTT ENSP00000500990.1:n.*1308_*1309insGTT
ENST00000673766.1:n.1986_1987insGTT
ENST00000673902.1:c.390+3874_390+3875insGTT ENSP00000501102.1:n.390+3874_390+3875insGTT
ENST00000336904.7:c.*1308_*1309insGTT ENSP00000338345.3:n.*1308_*1309insGTT
ENST00000394989.6:c.*1308_*1309insGTT ENSP00000378440.2:n.*1308_*1309insGTT
ENST00000420646.6:c.*1308_*1309insGTT ENSP00000396241.2:n.*1308_*1309insGTT
ENST00000618500.4:c.*1308_*1309insGTT ENSP00000484044.1:n.*1308_*1309insGTT
NM_000345.3:c.*1308_*1309insGTT NP_000336.1:n.*1308_*1309insGTT
NM_001146054.1:c.*1308_*1309insGTT NP_001139526.1:n.*1308_*1309insGTT
NM_001146055.1:c.*1308_*1309insGTT NP_001139527.1:n.*1308_*1309insGTT
NM_007308.2:c.*1308_*1309insGTT NP_009292.1:n.*1308_*1309insGTT
NM_000345.4:c.*1308_*1309insGTT MANE Select NP_000336.1:n.*1308_*1309insGTT
NM_001146054.2:c.*1308_*1309insGTT NP_001139526.1:n.*1308_*1309insGTT
NM_001146055.2:c.*1308_*1309insGTT NP_001139527.1:n.*1308_*1309insGTT
NM_001375285.1:c.*1308_*1309insGTT NP_001362214.1:n.*1308_*1309insGTT
NM_001375286.1:c.*1308_*1309insGTT NP_001362215.1:n.*1308_*1309insGTT
NM_001375287.1:c.*1308_*1309insGTT NP_001362216.1:n.*1308_*1309insGTT
NM_001375288.1:c.*1308_*1309insGTT NP_001362217.1:n.*1308_*1309insGTT
NM_001375290.1:c.*1308_*1309insGTT NP_001362219.1:n.*1308_*1309insGTT
NR_164674.1:n.1277-6_1277-5insGTT
NR_164675.1:n.1424-6_1424-5insGTT
NR_164676.1:n.2029_2030insGTT
NM_007308.3:c.*1308_*1309insGTT NP_009292.1:n.*1308_*1309insGTT