Canonical Allele Identifier: CA944538220
Gene: AICDA HGNC NCBI

Linked Data

gnomAD v3: 12-8604949-G-A
gnomAD v4: 12-8604949-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604949G>A , CM000674.2:g.8604949G>A GRCh38
NC_000012.11:g.8757545G>A , CM000674.1:g.8757545G>A GRCh37
NC_000012.10:g.8648812G>A NCBI36
NG_011588.1:g.12898C>T , LRG_17:g.12898C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.428-57C>T ENSP00000445691.1:n.428-57C>T
ENST00000543081.6:c.427+266C>T ENSP00000439103.2:n.427+266C>T
ENST00000544516.6:c.157-612C>T ENSP00000439538.2:n.157-612C>T
ENST00000545576.2:n.802C>T
ENST00000696246.1:c.413-57C>T ENSP00000512504.1:n.413-57C>T
ENST00000696271.1:n.813C>T
ENST00000696272.1:c.413-27C>T ENSP00000512515.1:n.413-27C>T
ENST00000696273.1:c.461-27C>T ENSP00000512516.1:n.461-27C>T
ENST00000229335.11:c.428-27C>T MANE Select ENSP00000229335.6:n.428-27C>T
ENST00000229335.10:c.428-27C>T ENSP00000229335.6:n.428-27C>T
ENST00000537228.5:c.428-57C>T ENSP00000445691.1:n.428-57C>T
ENST00000543081.5:c.423+266C>T
ENST00000544516.5:c.153-612C>T
ENST00000545512.1:c.424-27C>T
ENST00000545576.1:n.727C>T
NM_020661.2:c.428-27C>T , LRG_17t1:c.428-27C>T NP_065712.1:n.428-27C>T
XM_011520772.1:c.428-57C>T XP_011519074.1:n.428-57C>T
XM_011520773.1:c.427+266C>T XP_011519075.1:n.427+266C>T
NM_001330343.1:c.428-57C>T NP_001317272.1:n.428-57C>T
NM_020661.3:c.428-27C>T NP_065712.1:n.428-27C>T
XM_011520773.2:c.427+266C>T XP_011519075.1:n.427+266C>T
NM_020661.4:c.428-27C>T MANE Select NP_065712.1:n.428-27C>T
NM_001330343.2:c.428-57C>T NP_001317272.1:n.428-57C>T