Canonical Allele Identifier: CA692858926
Gene: AICDA HGNC NCBI

Linked Data

dbSNP Id: rs1475289166

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604523_8604524del , CM000674.2:g.8604523_8604524del GRCh38
NC_000012.11:g.8757119_8757120del , CM000674.1:g.8757119_8757120del GRCh37
NC_000012.10:g.8648386_8648387del NCBI36
NG_011588.1:g.13323_13324del , LRG_17:g.13323_13324del

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-187_514-186del ENSP00000445691.1:n.514-187_514-186del
ENST00000543081.6:c.428-187_428-186del ENSP00000439103.2:n.428-187_428-186del
ENST00000544516.6:c.157-187_157-186del ENSP00000439538.2:n.157-187_157-186del
ENST00000545576.2:n.945-187_945-186del
ENST00000696246.1:c.499-187_499-186del ENSP00000512504.1:n.499-187_499-186del
ENST00000696271.1:n.956-187_956-186del
ENST00000696272.1:c.529-187_529-186del ENSP00000512515.1:n.529-187_529-186del
ENST00000696273.1:c.577-187_577-186del ENSP00000512516.1:n.577-187_577-186del
ENST00000229335.11:c.544-187_544-186del MANE Select ENSP00000229335.6:n.544-187_544-186del
ENST00000229335.10:c.544-187_544-186del ENSP00000229335.6:n.544-187_544-186del
ENST00000537228.5:c.514-187_514-186del ENSP00000445691.1:n.514-187_514-186del
ENST00000543081.5:c.424-187_424-186del
ENST00000544516.5:c.153-187_153-186del
ENST00000545512.1:c.540-187_540-186del
ENST00000545576.1:n.870-187_870-186del
NM_020661.2:c.544-187_544-186del , LRG_17t1:c.544-187_544-186del NP_065712.1:n.544-187_544-186del
XM_011520772.1:c.514-187_514-186del XP_011519074.1:n.514-187_514-186del
XM_011520773.1:c.428-187_428-186del XP_011519075.1:n.428-187_428-186del
NM_001330343.1:c.514-187_514-186del NP_001317272.1:n.514-187_514-186del
NM_020661.3:c.544-187_544-186del NP_065712.1:n.544-187_544-186del
XM_011520773.2:c.428-187_428-186del XP_011519075.1:n.428-187_428-186del
NM_020661.4:c.544-187_544-186del MANE Select NP_065712.1:n.544-187_544-186del
NM_001330343.2:c.514-187_514-186del NP_001317272.1:n.514-187_514-186del