Canonical Allele Identifier: CA2015111928
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8606919C= , CM000674.2:g.8606919C= GRCh38
NC_000012.11:g.8759515C= , CM000674.1:g.8759515C= GRCh37
NC_000012.10:g.8650782C= NCBI36
NG_011588.1:g.10928G= , LRG_17:g.10928G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.102G= ENSP00000445691.1:p.Lys34=
ENST00000543081.6:c.102G= ENSP00000439103.2:p.Lys34=
ENST00000544516.6:c.102G= ENSP00000439538.2:p.Lys34=
ENST00000545576.2:n.211G=
ENST00000696246.1:c.87G= ENSP00000512504.1:p.Lys29=
ENST00000696271.1:n.222G=
ENST00000696272.1:c.87G= ENSP00000512515.1:p.Lys29=
ENST00000696273.1:c.135G= ENSP00000512516.1:p.Lys45=
ENST00000229335.11:c.102G= MANE Select ENSP00000229335.6:p.Lys34=
ENST00000229335.10:c.102G= ENSP00000229335.6:p.Lys34=
ENST00000537228.5:c.102G= ENSP00000445691.1:p.Lys34=
ENST00000543081.5:c.98G=
ENST00000544516.5:c.98G=
ENST00000545512.1:c.98G=
ENST00000545576.1:n.136G=
NM_020661.2:c.102G= , LRG_17t1:c.102G= NP_065712.1:p.Lys34=
XM_011520772.1:c.102G= XP_011519074.1:p.Lys34=
XM_011520773.1:c.102G= XP_011519075.1:p.Lys34=
NM_001330343.1:c.102G= NP_001317272.1:p.Lys34=
NM_020661.3:c.102G= NP_065712.1:p.Lys34=
XM_011520773.2:c.102G= XP_011519075.1:p.Lys34=
NM_020661.4:c.102G= MANE Select NP_065712.1:p.Lys34=
NM_001330343.2:c.102G= NP_001317272.1:p.Lys34=