Canonical Allele Identifier: CA692858917
Gene: AICDA HGNC NCBI

Linked Data

dbSNP Id: rs1164551368

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604517_8604524del , CM000674.2:g.8604517_8604524del GRCh38
NC_000012.11:g.8757113_8757120del , CM000674.1:g.8757113_8757120del GRCh37
NC_000012.10:g.8648380_8648387del NCBI36
NG_011588.1:g.13323_13330del , LRG_17:g.13323_13330del

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-187_514-180del ENSP00000445691.1:n.514-187_514-180del
ENST00000543081.6:c.428-187_428-180del ENSP00000439103.2:n.428-187_428-180del
ENST00000544516.6:c.157-187_157-180del ENSP00000439538.2:n.157-187_157-180del
ENST00000545576.2:n.945-187_945-180del
ENST00000696246.1:c.499-187_499-180del ENSP00000512504.1:n.499-187_499-180del
ENST00000696271.1:n.956-187_956-180del
ENST00000696272.1:c.529-187_529-180del ENSP00000512515.1:n.529-187_529-180del
ENST00000696273.1:c.577-187_577-180del ENSP00000512516.1:n.577-187_577-180del
ENST00000229335.11:c.544-187_544-180del MANE Select ENSP00000229335.6:n.544-187_544-180del
ENST00000229335.10:c.544-187_544-180del ENSP00000229335.6:n.544-187_544-180del
ENST00000537228.5:c.514-187_514-180del ENSP00000445691.1:n.514-187_514-180del
ENST00000543081.5:c.424-187_424-180del
ENST00000544516.5:c.153-187_153-180del
ENST00000545512.1:c.540-187_540-180del
ENST00000545576.1:n.870-187_870-180del
NM_020661.2:c.544-187_544-180del , LRG_17t1:c.544-187_544-180del NP_065712.1:n.544-187_544-180del
XM_011520772.1:c.514-187_514-180del XP_011519074.1:n.514-187_514-180del
XM_011520773.1:c.428-187_428-180del XP_011519075.1:n.428-187_428-180del
NM_001330343.1:c.514-187_514-180del NP_001317272.1:n.514-187_514-180del
NM_020661.3:c.544-187_544-180del NP_065712.1:n.544-187_544-180del
XM_011520773.2:c.428-187_428-180del XP_011519075.1:n.428-187_428-180del
NM_020661.4:c.544-187_544-180del MANE Select NP_065712.1:n.544-187_544-180del
NM_001330343.2:c.514-187_514-180del NP_001317272.1:n.514-187_514-180del