Canonical Allele Identifier: CA2794483207
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604476_8604478del , CM000674.2:g.8604476_8604478del GRCh38
NC_000012.11:g.8757072_8757074del , CM000674.1:g.8757072_8757074del GRCh37
NC_000012.10:g.8648339_8648341del NCBI36
NG_011588.1:g.13369_13371del , LRG_17:g.13369_13371del

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-141_514-139del ENSP00000445691.1:n.514-141_514-139del
ENST00000543081.6:c.428-141_428-139del ENSP00000439103.2:n.428-141_428-139del
ENST00000544516.6:c.157-141_157-139del ENSP00000439538.2:n.157-141_157-139del
ENST00000545576.2:n.945-141_945-139del
ENST00000696246.1:c.499-141_499-139del ENSP00000512504.1:n.499-141_499-139del
ENST00000696271.1:n.956-141_956-139del
ENST00000696272.1:c.529-141_529-139del ENSP00000512515.1:n.529-141_529-139del
ENST00000696273.1:c.577-141_577-139del ENSP00000512516.1:n.577-141_577-139del
ENST00000229335.11:c.544-141_544-139del MANE Select ENSP00000229335.6:n.544-141_544-139del
ENST00000229335.10:c.544-141_544-139del ENSP00000229335.6:n.544-141_544-139del
ENST00000537228.5:c.514-141_514-139del ENSP00000445691.1:n.514-141_514-139del
ENST00000543081.5:c.424-141_424-139del
ENST00000544516.5:c.153-141_153-139del
ENST00000545512.1:c.540-141_540-139del
ENST00000545576.1:n.870-141_870-139del
NM_020661.2:c.544-141_544-139del , LRG_17t1:c.544-141_544-139del NP_065712.1:n.544-141_544-139del
XM_011520772.1:c.514-141_514-139del XP_011519074.1:n.514-141_514-139del
XM_011520773.1:c.428-141_428-139del XP_011519075.1:n.428-141_428-139del
NM_001330343.1:c.514-141_514-139del NP_001317272.1:n.514-141_514-139del
NM_020661.3:c.544-141_544-139del NP_065712.1:n.544-141_544-139del
XM_011520773.2:c.428-141_428-139del XP_011519075.1:n.428-141_428-139del
NM_020661.4:c.544-141_544-139del MANE Select NP_065712.1:n.544-141_544-139del
NM_001330343.2:c.514-141_514-139del NP_001317272.1:n.514-141_514-139del