Canonical Allele Identifier: CA944538102
Gene: AICDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604912_8604913del , CM000674.2:g.8604912_8604913del GRCh38
NC_000012.11:g.8757508_8757509del , CM000674.1:g.8757508_8757509del GRCh37
NC_000012.10:g.8648775_8648776del NCBI36
NG_011588.1:g.12934_12935del , LRG_17:g.12934_12935del

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.428-21_428-20del ENSP00000445691.1:n.428-21_428-20del
ENST00000543081.6:c.427+302_427+303del ENSP00000439103.2:n.427+302_427+303del
ENST00000544516.6:c.157-576_157-575del ENSP00000439538.2:n.157-576_157-575del
ENST00000545576.2:n.838_839del
ENST00000696246.1:c.413-21_413-20del ENSP00000512504.1:n.413-21_413-20del
ENST00000696271.1:n.849_850del
ENST00000696272.1:c.422_423del ENSP00000512515.1:p.Tyr141LeufsTer21
ENST00000696273.1:c.470_471del ENSP00000512516.1:p.Tyr157LeufsTer21
ENST00000229335.11:c.437_438del MANE Select ENSP00000229335.6:p.Tyr146LeufsTer21
ENST00000229335.10:c.437_438del ENSP00000229335.6:p.Tyr146LeufsTer21
ENST00000537228.5:c.428-21_428-20del ENSP00000445691.1:n.428-21_428-20del
ENST00000543081.5:c.423+302_423+303del
ENST00000544516.5:c.153-576_153-575del
ENST00000545512.1:c.433_434del
ENST00000545576.1:n.763_764del
NM_020661.2:c.437_438del , LRG_17t1:c.437_438del NP_065712.1:p.Tyr146LeufsTer21
XM_011520772.1:c.428-21_428-20del XP_011519074.1:n.428-21_428-20del
XM_011520773.1:c.427+302_427+303del XP_011519075.1:n.427+302_427+303del
NM_001330343.1:c.428-21_428-20del NP_001317272.1:n.428-21_428-20del
NM_020661.3:c.437_438del NP_065712.1:p.Tyr146LeufsTer21
XM_011520773.2:c.427+302_427+303del XP_011519075.1:n.427+302_427+303del
NM_020661.4:c.437_438del MANE Select NP_065712.1:p.Tyr146LeufsTer21
NM_001330343.2:c.428-21_428-20del NP_001317272.1:n.428-21_428-20del