Canonical Allele Identifier: CA1475384952
Community Standard Title: NC_000004.12:g.89837238G=
Gene: SNCA HGNC NCBI
SNCA-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89837238G= , CM000666.2:g.89837238G= GRCh38
NC_000004.11:g.90758389G= , CM000666.1:g.90758389G= GRCh37
NC_000004.10:g.90977412G= NCBI36
NG_011851.1:g.6059C=

Transcript Alleles

HGVS Amino-acid Change
NM_001146055.1:c.-26+1014C= (SNCA) NP_001139527.1:n.-26+1014C=
NM_001146055.2:c.-26+1014C= (SNCA) NP_001139527.1:n.-26+1014C=
NM_001375285.1:c.-94-709C= (SNCA) NP_001362214.1:n.-94-709C=
NR_045481.1:n.334+504G= (SNCA-AS1)
NR_164674.1:n.53+1014C= (SNCA)
ENST00000336904.7:c.-26+1014C= (SNCA) ENSP00000338345.3:n.-26+1014C=
ENST00000673902.1:c.-302C= (SNCA) ENSP00000501102.1:n.-302C=
ENST00000674129.1:c.-302C= (SNCA) ENSP00000501269.1:n.-302C=
XM_011532205.1:c.-26+1014C= (SNCA) XP_011530507.1:n.-26+1014C=
XM_011532205.2:c.-26+1014C= (SNCA) XP_011530507.1:n.-26+1014C=