Canonical Allele Identifier: CA692858800
Gene: AICDA HGNC NCBI

Linked Data

dbSNP Id: rs1348536796

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604493_8604501del , CM000674.2:g.8604493_8604501del GRCh38
NC_000012.11:g.8757089_8757097del , CM000674.1:g.8757089_8757097del GRCh37
NC_000012.10:g.8648356_8648364del NCBI36
NG_011588.1:g.13346_13354del , LRG_17:g.13346_13354del

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-164_514-156del ENSP00000445691.1:n.514-164_514-156del
ENST00000543081.6:c.428-164_428-156del ENSP00000439103.2:n.428-164_428-156del
ENST00000544516.6:c.157-164_157-156del ENSP00000439538.2:n.157-164_157-156del
ENST00000545576.2:n.945-164_945-156del
ENST00000696246.1:c.499-164_499-156del ENSP00000512504.1:n.499-164_499-156del
ENST00000696271.1:n.956-164_956-156del
ENST00000696272.1:c.529-164_529-156del ENSP00000512515.1:n.529-164_529-156del
ENST00000696273.1:c.577-164_577-156del ENSP00000512516.1:n.577-164_577-156del
ENST00000229335.11:c.544-164_544-156del MANE Select ENSP00000229335.6:n.544-164_544-156del
ENST00000229335.10:c.544-164_544-156del ENSP00000229335.6:n.544-164_544-156del
ENST00000537228.5:c.514-164_514-156del ENSP00000445691.1:n.514-164_514-156del
ENST00000543081.5:c.424-164_424-156del
ENST00000544516.5:c.153-164_153-156del
ENST00000545512.1:c.540-164_540-156del
ENST00000545576.1:n.870-164_870-156del
NM_020661.2:c.544-164_544-156del , LRG_17t1:c.544-164_544-156del NP_065712.1:n.544-164_544-156del
XM_011520772.1:c.514-164_514-156del XP_011519074.1:n.514-164_514-156del
XM_011520773.1:c.428-164_428-156del XP_011519075.1:n.428-164_428-156del
NM_001330343.1:c.514-164_514-156del NP_001317272.1:n.514-164_514-156del
NM_020661.3:c.544-164_544-156del NP_065712.1:n.544-164_544-156del
XM_011520773.2:c.428-164_428-156del XP_011519075.1:n.428-164_428-156del
NM_020661.4:c.544-164_544-156del MANE Select NP_065712.1:n.544-164_544-156del
NM_001330343.2:c.514-164_514-156del NP_001317272.1:n.514-164_514-156del