Canonical Allele Identifier: CA2617496782
Gene: AICDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8606889del , CM000674.2:g.8606889del GRCh38
NC_000012.11:g.8759485del , CM000674.1:g.8759485del GRCh37
NC_000012.10:g.8650752del NCBI36
NG_011588.1:g.10959del , LRG_17:g.10959del

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.133del ENSP00000445691.1:p.Asp45ThrfsTer26
ENST00000543081.6:c.133del ENSP00000439103.2:p.Asp45ThrfsTer26
ENST00000544516.6:c.133del ENSP00000439538.2:p.Asp45ThrfsTer?
ENST00000545576.2:n.242del
ENST00000696246.1:c.118del ENSP00000512504.1:p.Asp40ThrfsTer26
ENST00000696271.1:n.253del
ENST00000696272.1:c.118del ENSP00000512515.1:p.Asp40ThrfsTer26
ENST00000696273.1:c.166del ENSP00000512516.1:p.Asp56ThrfsTer26
ENST00000229335.11:c.133del MANE Select ENSP00000229335.6:p.Asp45ThrfsTer26
ENST00000229335.10:c.133del ENSP00000229335.6:p.Asp45ThrfsTer26
ENST00000537228.5:c.133del ENSP00000445691.1:p.Asp45ThrfsTer26
ENST00000543081.5:c.129del
ENST00000544516.5:c.129del
ENST00000545512.1:c.129del
ENST00000545576.1:n.167del
NM_020661.2:c.133del , LRG_17t1:c.133del NP_065712.1:p.Asp45ThrfsTer26
XM_011520772.1:c.133del XP_011519074.1:p.Asp45ThrfsTer26
XM_011520773.1:c.133del XP_011519075.1:p.Asp45ThrfsTer26
NM_001330343.1:c.133del NP_001317272.1:p.Asp45ThrfsTer26
NM_020661.3:c.133del NP_065712.1:p.Asp45ThrfsTer26
XM_011520773.2:c.133del XP_011519075.1:p.Asp45ThrfsTer26
NM_020661.4:c.133del MANE Select NP_065712.1:p.Asp45ThrfsTer26
NM_001330343.2:c.133del NP_001317272.1:p.Asp45ThrfsTer26