Canonical Allele Identifier: CA799760887

Gene: SNCA

Linked Data

• dbSNP Id: rs1329167346
• MyVariant Identifiers: chr4:g.90646556T>C (hg19) ; chr4:g.89725405T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89725405T>C , CM000666.2:g.89725405T>C	GRCh38
NC_000004.11:g.90646556T>C , CM000666.1:g.90646556T>C	GRCh37
NC_000004.10:g.90865579T>C	NCBI36
NG_011851.1:g.117892A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394991.8:c.*1223A>G MANE Select	ENSP00000378442.4:n.*1223A>G
ENST00000673718.1:c.*1223A>G	ENSP00000500990.1:n.*1223A>G
ENST00000673766.1:n.1901A>G
ENST00000673902.1:c.390+3789A>G	ENSP00000501102.1:n.390+3789A>G
ENST00000674129.1:c.*1223A>G	ENSP00000501269.1:n.*1223A>G
ENST00000336904.7:c.*1223A>G	ENSP00000338345.3:n.*1223A>G
ENST00000394989.6:c.*1223A>G	ENSP00000378440.2:n.*1223A>G
ENST00000420646.6:c.*1223A>G	ENSP00000396241.2:n.*1223A>G
ENST00000618500.4:c.*1223A>G	ENSP00000484044.1:n.*1223A>G
NM_000345.3:c.*1223A>G	NP_000336.1:n.*1223A>G
NM_001146054.1:c.*1223A>G	NP_001139526.1:n.*1223A>G
NM_001146055.1:c.*1223A>G	NP_001139527.1:n.*1223A>G
NM_007308.2:c.*1223A>G	NP_009292.1:n.*1223A>G
NM_000345.4:c.*1223A>G MANE Select	NP_000336.1:n.*1223A>G
NM_001146054.2:c.*1223A>G	NP_001139526.1:n.*1223A>G
NM_001146055.2:c.*1223A>G	NP_001139527.1:n.*1223A>G
NM_001375285.1:c.*1223A>G	NP_001362214.1:n.*1223A>G
NM_001375286.1:c.*1223A>G	NP_001362215.1:n.*1223A>G
NM_001375287.1:c.*1223A>G	NP_001362216.1:n.*1223A>G
NM_001375288.1:c.*1223A>G	NP_001362217.1:n.*1223A>G
NM_001375290.1:c.*1223A>G	NP_001362219.1:n.*1223A>G
NR_164674.1:n.1277-91A>G
NR_164675.1:n.1424-91A>G
NR_164676.1:n.1944A>G
NM_007308.3:c.*1223A>G	NP_009292.1:n.*1223A>G