Canonical Allele Identifier: CA944538194
Gene: AICDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604934_8604939dup , CM000674.2:g.8604934_8604939dup GRCh38
NC_000012.11:g.8757530_8757535dup , CM000674.1:g.8757530_8757535dup GRCh37
NC_000012.10:g.8648797_8648802dup NCBI36
NG_011588.1:g.12915_12920dup , LRG_17:g.12915_12920dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.428-40_428-35dup ENSP00000445691.1:n.428-40_428-35dup
ENST00000543081.6:c.427+283_427+288dup ENSP00000439103.2:n.427+283_427+288dup
ENST00000544516.6:c.157-595_157-590dup ENSP00000439538.2:n.157-595_157-590dup
ENST00000545576.2:n.819_824dup
ENST00000696246.1:c.413-40_413-35dup ENSP00000512504.1:n.413-40_413-35dup
ENST00000696271.1:n.830_835dup
ENST00000696272.1:c.413-10_413-5dup ENSP00000512515.1:n.413-10_413-5dup
ENST00000696273.1:c.461-10_461-5dup ENSP00000512516.1:n.461-10_461-5dup
ENST00000229335.11:c.428-10_428-5dup MANE Select ENSP00000229335.6:n.428-10_428-5dup
ENST00000229335.10:c.428-10_428-5dup ENSP00000229335.6:n.428-10_428-5dup
ENST00000537228.5:c.428-40_428-35dup ENSP00000445691.1:n.428-40_428-35dup
ENST00000543081.5:c.423+283_423+288dup
ENST00000544516.5:c.153-595_153-590dup
ENST00000545512.1:c.424-10_424-5dup
ENST00000545576.1:n.744_749dup
NM_020661.2:c.428-10_428-5dup , LRG_17t1:c.428-10_428-5dup NP_065712.1:n.428-10_428-5dup
XM_011520772.1:c.428-40_428-35dup XP_011519074.1:n.428-40_428-35dup
XM_011520773.1:c.427+283_427+288dup XP_011519075.1:n.427+283_427+288dup
NM_001330343.1:c.428-40_428-35dup NP_001317272.1:n.428-40_428-35dup
NM_020661.3:c.428-10_428-5dup NP_065712.1:n.428-10_428-5dup
XM_011520773.2:c.427+283_427+288dup XP_011519075.1:n.427+283_427+288dup
NM_020661.4:c.428-10_428-5dup MANE Select NP_065712.1:n.428-10_428-5dup
NM_001330343.2:c.428-40_428-35dup NP_001317272.1:n.428-40_428-35dup