Canonical Allele Identifier: CA944537920
Gene: AICDA HGNC NCBI

Linked Data

gnomAD v3: 12-8604587-T-A
gnomAD v4: 12-8604587-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604587T>A , CM000674.2:g.8604587T>A GRCh38
NC_000012.11:g.8757183T>A , CM000674.1:g.8757183T>A GRCh37
NC_000012.10:g.8648450T>A NCBI36
NG_011588.1:g.13260A>T , LRG_17:g.13260A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.513+220A>T ENSP00000445691.1:n.513+220A>T
ENST00000543081.6:c.428-250A>T ENSP00000439103.2:n.428-250A>T
ENST00000544516.6:c.157-250A>T ENSP00000439538.2:n.157-250A>T
ENST00000545576.2:n.944+220A>T
ENST00000696246.1:c.498+220A>T ENSP00000512504.1:n.498+220A>T
ENST00000696271.1:n.955+220A>T
ENST00000696272.1:c.528+220A>T ENSP00000512515.1:n.528+220A>T
ENST00000696273.1:c.576+220A>T ENSP00000512516.1:n.576+220A>T
ENST00000229335.11:c.543+220A>T MANE Select ENSP00000229335.6:n.543+220A>T
ENST00000229335.10:c.543+220A>T ENSP00000229335.6:n.543+220A>T
ENST00000537228.5:c.513+220A>T ENSP00000445691.1:n.513+220A>T
ENST00000543081.5:c.424-250A>T
ENST00000544516.5:c.153-250A>T
ENST00000545512.1:c.539+220A>T
ENST00000545576.1:n.869+220A>T
NM_020661.2:c.543+220A>T , LRG_17t1:c.543+220A>T NP_065712.1:n.543+220A>T
XM_011520772.1:c.513+220A>T XP_011519074.1:n.513+220A>T
XM_011520773.1:c.428-250A>T XP_011519075.1:n.428-250A>T
NM_001330343.1:c.513+220A>T NP_001317272.1:n.513+220A>T
NM_020661.3:c.543+220A>T NP_065712.1:n.543+220A>T
XM_011520773.2:c.428-250A>T XP_011519075.1:n.428-250A>T
NM_020661.4:c.543+220A>T MANE Select NP_065712.1:n.543+220A>T
NM_001330343.2:c.513+220A>T NP_001317272.1:n.513+220A>T