Canonical Allele Identifier: CA117277
Gene: AICDA HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 5127
ClinVar RCV Id: RCV000005434
dbSNP Id: rs104894323

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604909G>T , CM000674.2:g.8604909G>T GRCh38
NC_000012.11:g.8757505G>T , CM000674.1:g.8757505G>T GRCh37
NC_000012.10:g.8648772G>T NCBI36
NG_011588.1:g.12938C>A , LRG_17:g.12938C>A

Transcript Alleles

HGVS Amino-acid change
NM_020661.2:c.441C>A , LRG_17t1:c.441C>A NP_065712.1:p.Cys147Ter
XM_011520772.1:c.428-17C>A XP_011519074.1:p.=
XM_011520773.1:c.427+306C>A XP_011519075.1:p.=
NM_001330343.1:c.428-17C>A VV NP_001317272.1:p.=
NM_020661.3:c.441C>A VV NP_065712.1:p.Cys147Ter
XM_011520773.2:c.427+306C>A XP_011519075.1:p.=
NM_020661.4:c.441C>A VV MANE Preferred NP_065712.1:p.Cys147Ter
ENST00000229335.10:c.441C>A ENSP00000229335.6:p.Cys147Ter
ENST00000537228.5:c.428-17C>A ENSP00000445691.1:p.=
ENST00000543081.5:n.423+306C>A
ENST00000544516.5:n.153-572C>A
ENST00000545512.1:n.437C>A
ENST00000545576.1:n.767C>A