Canonical Allele Identifier: CA692858829
Gene: AICDA HGNC NCBI

Linked Data

dbSNP Id: rs374498877

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604514_8604523del , CM000674.2:g.8604514_8604523del GRCh38
NC_000012.11:g.8757110_8757119del , CM000674.1:g.8757110_8757119del GRCh37
NC_000012.10:g.8648377_8648386del NCBI36
NG_011588.1:g.13341_13350del , LRG_17:g.13341_13350del

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-169_514-160del ENSP00000445691.1:n.514-169_514-160del
ENST00000543081.6:c.428-169_428-160del ENSP00000439103.2:n.428-169_428-160del
ENST00000544516.6:c.157-169_157-160del ENSP00000439538.2:n.157-169_157-160del
ENST00000545576.2:n.945-169_945-160del
ENST00000696246.1:c.499-169_499-160del ENSP00000512504.1:n.499-169_499-160del
ENST00000696271.1:n.956-169_956-160del
ENST00000696272.1:c.529-169_529-160del ENSP00000512515.1:n.529-169_529-160del
ENST00000696273.1:c.577-169_577-160del ENSP00000512516.1:n.577-169_577-160del
ENST00000229335.11:c.544-169_544-160del MANE Select ENSP00000229335.6:n.544-169_544-160del
ENST00000229335.10:c.544-169_544-160del ENSP00000229335.6:n.544-169_544-160del
ENST00000537228.5:c.514-169_514-160del ENSP00000445691.1:n.514-169_514-160del
ENST00000543081.5:c.424-169_424-160del
ENST00000544516.5:c.153-169_153-160del
ENST00000545512.1:c.540-169_540-160del
ENST00000545576.1:n.870-169_870-160del
NM_020661.2:c.544-169_544-160del , LRG_17t1:c.544-169_544-160del NP_065712.1:n.544-169_544-160del
XM_011520772.1:c.514-169_514-160del XP_011519074.1:n.514-169_514-160del
XM_011520773.1:c.428-169_428-160del XP_011519075.1:n.428-169_428-160del
NM_001330343.1:c.514-169_514-160del NP_001317272.1:n.514-169_514-160del
NM_020661.3:c.544-169_544-160del NP_065712.1:n.544-169_544-160del
XM_011520773.2:c.428-169_428-160del XP_011519075.1:n.428-169_428-160del
NM_020661.4:c.544-169_544-160del MANE Select NP_065712.1:n.544-169_544-160del
NM_001330343.2:c.514-169_514-160del NP_001317272.1:n.514-169_514-160del