Canonical Allele Identifier: CA692858790
Gene: AICDA HGNC NCBI

Linked Data

dbSNP Id: rs1215876534

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604493_8604496dup , CM000674.2:g.8604493_8604496dup GRCh38
NC_000012.11:g.8757089_8757092dup , CM000674.1:g.8757089_8757092dup GRCh37
NC_000012.10:g.8648356_8648359dup NCBI36
NG_011588.1:g.13362_13365dup , LRG_17:g.13362_13365dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-148_514-145dup ENSP00000445691.1:n.514-148_514-145dup
ENST00000543081.6:c.428-148_428-145dup ENSP00000439103.2:n.428-148_428-145dup
ENST00000544516.6:c.157-148_157-145dup ENSP00000439538.2:n.157-148_157-145dup
ENST00000545576.2:n.945-148_945-145dup
ENST00000696246.1:c.499-148_499-145dup ENSP00000512504.1:n.499-148_499-145dup
ENST00000696271.1:n.956-148_956-145dup
ENST00000696272.1:c.529-148_529-145dup ENSP00000512515.1:n.529-148_529-145dup
ENST00000696273.1:c.577-148_577-145dup ENSP00000512516.1:n.577-148_577-145dup
ENST00000229335.11:c.544-148_544-145dup MANE Select ENSP00000229335.6:n.544-148_544-145dup
ENST00000229335.10:c.544-148_544-145dup ENSP00000229335.6:n.544-148_544-145dup
ENST00000537228.5:c.514-148_514-145dup ENSP00000445691.1:n.514-148_514-145dup
ENST00000543081.5:c.424-148_424-145dup
ENST00000544516.5:c.153-148_153-145dup
ENST00000545512.1:c.540-148_540-145dup
ENST00000545576.1:n.870-148_870-145dup
NM_020661.2:c.544-148_544-145dup , LRG_17t1:c.544-148_544-145dup NP_065712.1:n.544-148_544-145dup
XM_011520772.1:c.514-148_514-145dup XP_011519074.1:n.514-148_514-145dup
XM_011520773.1:c.428-148_428-145dup XP_011519075.1:n.428-148_428-145dup
NM_001330343.1:c.514-148_514-145dup NP_001317272.1:n.514-148_514-145dup
NM_020661.3:c.544-148_544-145dup NP_065712.1:n.544-148_544-145dup
XM_011520773.2:c.428-148_428-145dup XP_011519075.1:n.428-148_428-145dup
NM_020661.4:c.544-148_544-145dup MANE Select NP_065712.1:n.544-148_544-145dup
NM_001330343.2:c.514-148_514-145dup NP_001317272.1:n.514-148_514-145dup