Canonical Allele Identifier: CA944537755
Gene: AICDA HGNC NCBI

Linked Data

dbSNP Id: rs993737872
gnomAD v3: 12-8604523-A-T
gnomAD v4: 12-8604523-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604523A>T , CM000674.2:g.8604523A>T GRCh38
NC_000012.11:g.8757119A>T , CM000674.1:g.8757119A>T GRCh37
NC_000012.10:g.8648386A>T NCBI36
NG_011588.1:g.13324T>A , LRG_17:g.13324T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-186T>A ENSP00000445691.1:n.514-186T>A
ENST00000543081.6:c.428-186T>A ENSP00000439103.2:n.428-186T>A
ENST00000544516.6:c.157-186T>A ENSP00000439538.2:n.157-186T>A
ENST00000545576.2:n.945-186T>A
ENST00000696246.1:c.499-186T>A ENSP00000512504.1:n.499-186T>A
ENST00000696271.1:n.956-186T>A
ENST00000696272.1:c.529-186T>A ENSP00000512515.1:n.529-186T>A
ENST00000696273.1:c.577-186T>A ENSP00000512516.1:n.577-186T>A
ENST00000229335.11:c.544-186T>A MANE Select ENSP00000229335.6:n.544-186T>A
ENST00000229335.10:c.544-186T>A ENSP00000229335.6:n.544-186T>A
ENST00000537228.5:c.514-186T>A ENSP00000445691.1:n.514-186T>A
ENST00000543081.5:c.424-186T>A
ENST00000544516.5:c.153-186T>A
ENST00000545512.1:c.540-186T>A
ENST00000545576.1:n.870-186T>A
NM_020661.2:c.544-186T>A , LRG_17t1:c.544-186T>A NP_065712.1:n.544-186T>A
XM_011520772.1:c.514-186T>A XP_011519074.1:n.514-186T>A
XM_011520773.1:c.428-186T>A XP_011519075.1:n.428-186T>A
NM_001330343.1:c.514-186T>A NP_001317272.1:n.514-186T>A
NM_020661.3:c.544-186T>A NP_065712.1:n.544-186T>A
XM_011520773.2:c.428-186T>A XP_011519075.1:n.428-186T>A
NM_020661.4:c.544-186T>A MANE Select NP_065712.1:n.544-186T>A
NM_001330343.2:c.514-186T>A NP_001317272.1:n.514-186T>A