Canonical Allele Identifier: CA944537789
Gene: AICDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604526_8604527insAAA , CM000674.2:g.8604526_8604527insAAA GRCh38
NC_000012.11:g.8757122_8757123insAAA , CM000674.1:g.8757122_8757123insAAA GRCh37
NC_000012.10:g.8648389_8648390insAAA NCBI36
NG_011588.1:g.13321_13322insTTT , LRG_17:g.13321_13322insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-189_514-188insTTT ENSP00000445691.1:n.514-189_514-188insTTT
ENST00000543081.6:c.428-189_428-188insTTT ENSP00000439103.2:n.428-189_428-188insTTT
ENST00000544516.6:c.157-189_157-188insTTT ENSP00000439538.2:n.157-189_157-188insTTT
ENST00000545576.2:n.945-189_945-188insTTT
ENST00000696246.1:c.499-189_499-188insTTT ENSP00000512504.1:n.499-189_499-188insTTT
ENST00000696271.1:n.956-189_956-188insTTT
ENST00000696272.1:c.529-189_529-188insTTT ENSP00000512515.1:n.529-189_529-188insTTT
ENST00000696273.1:c.577-189_577-188insTTT ENSP00000512516.1:n.577-189_577-188insTTT
ENST00000229335.11:c.544-189_544-188insTTT MANE Select ENSP00000229335.6:n.544-189_544-188insTTT
ENST00000229335.10:c.544-189_544-188insTTT ENSP00000229335.6:n.544-189_544-188insTTT
ENST00000537228.5:c.514-189_514-188insTTT ENSP00000445691.1:n.514-189_514-188insTTT
ENST00000543081.5:c.424-189_424-188insTTT
ENST00000544516.5:c.153-189_153-188insTTT
ENST00000545512.1:c.540-189_540-188insTTT
ENST00000545576.1:n.870-189_870-188insTTT
NM_020661.2:c.544-189_544-188insTTT , LRG_17t1:c.544-189_544-188insTTT NP_065712.1:n.544-189_544-188insTTT
XM_011520772.1:c.514-189_514-188insTTT XP_011519074.1:n.514-189_514-188insTTT
XM_011520773.1:c.428-189_428-188insTTT XP_011519075.1:n.428-189_428-188insTTT
NM_001330343.1:c.514-189_514-188insTTT NP_001317272.1:n.514-189_514-188insTTT
NM_020661.3:c.544-189_544-188insTTT NP_065712.1:n.544-189_544-188insTTT
XM_011520773.2:c.428-189_428-188insTTT XP_011519075.1:n.428-189_428-188insTTT
NM_020661.4:c.544-189_544-188insTTT MANE Select NP_065712.1:n.544-189_544-188insTTT
NM_001330343.2:c.514-189_514-188insTTT NP_001317272.1:n.514-189_514-188insTTT