Canonical Allele Identifier: CA1065251754

Gene: SNCA

Linked Data

• dbSNP Id: rs397994464
• gnomAD v3: 4-89725318-T-TAAAAAAAAAAAAAAAAAAAAA
• gnomAD v4: 4-89725318-T-TAAAAAAAAAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89725335_89725336insAAAAAAAAAAAAAAAAAAAAA , CM000666.2:g.89725335_89725336insAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000004.11:g.90646486_90646487insAAAAAAAAAAAAAAAAAAAAA , CM000666.1:g.90646486_90646487insAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000004.10:g.90865509_90865510insAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_011851.1:g.117978_117979insTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394991.8:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000378442.4:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
ENST00000673718.1:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	ENSP00000500990.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
ENST00000673766.1:n.1987_1988insTTTTTTTTTTTTTTTTTTTTT
ENST00000673902.1:c.390+3875_390+3876insTTTTTTTTTTTTTTTTTTTTT	ENSP00000501102.1:n.390+3875_390+3876insTTTTTTTTTTTTTTTTTTTTT...
ENST00000336904.7:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	ENSP00000338345.3:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
ENST00000394989.6:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	ENSP00000378440.2:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
ENST00000420646.6:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	ENSP00000396241.2:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
ENST00000618500.4:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	ENSP00000484044.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_000345.3:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_000336.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_001146054.1:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_001139526.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_001146055.1:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_001139527.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_007308.2:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_009292.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_000345.4:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_000336.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_001146054.2:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_001139526.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_001146055.2:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_001139527.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_001375285.1:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_001362214.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_001375286.1:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_001362215.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_001375287.1:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_001362216.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_001375288.1:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_001362217.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NM_001375290.1:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_001362219.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT
NR_164674.1:n.1277-5_1277-4insTTTTTTTTTTTTTTTTTTTTT
NR_164675.1:n.1424-5_1424-4insTTTTTTTTTTTTTTTTTTTTT
NR_164676.1:n.2030_2031insTTTTTTTTTTTTTTTTTTTTT
NM_007308.3:c.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT	NP_009292.1:n.*1309_*1310insTTTTTTTTTTTTTTTTTTTTT