Canonical Allele Identifier: CA1065254469
Gene: SNCA HGNC NCBI
SNCA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1739588119
gnomAD v3: 4-89837831-CAGG-C
gnomAD v4: 4-89837831-CAGG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89837834_89837836del , CM000666.2:g.89837834_89837836del GRCh38
NC_000004.11:g.90758985_90758987del , CM000666.1:g.90758985_90758987del GRCh37
NC_000004.10:g.90978008_90978010del NCBI36
NG_011851.1:g.5463_5465del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336904.7:c.-26+418_-26+420del (SNCA) ENSP00000338345.3:n.-26+418_-26+420del
NM_001146055.1:c.-26+418_-26+420del (SNCA) NP_001139527.1:n.-26+418_-26+420del
NR_045481.1:n.335-427_335-425del (SNCA-AS1)
XM_011532205.1:c.-26+418_-26+420del (SNCA) XP_011530507.1:n.-26+418_-26+420del
XM_011532205.2:c.-26+418_-26+420del (SNCA) XP_011530507.1:n.-26+418_-26+420del
NM_001146055.2:c.-26+418_-26+420del (SNCA) NP_001139527.1:n.-26+418_-26+420del
NM_001375285.1:c.-95+418_-95+420del (SNCA) NP_001362214.1:n.-95+418_-95+420del
NR_164674.1:n.53+418_53+420del (SNCA)
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