Canonical Allele Identifier: CA2015109828
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604922T= , CM000674.2:g.8604922T= GRCh38
NC_000012.11:g.8757518T= , CM000674.1:g.8757518T= GRCh37
NC_000012.10:g.8648785T= NCBI36
NG_011588.1:g.12925A= , LRG_17:g.12925A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.428-30A= ENSP00000445691.1:n.428-30A=
ENST00000543081.6:c.427+293A= ENSP00000439103.2:n.427+293A=
ENST00000544516.6:c.157-585A= ENSP00000439538.2:n.157-585A=
ENST00000545576.2:n.829A=
ENST00000696246.1:c.413-30A= ENSP00000512504.1:n.413-30A=
ENST00000696271.1:n.840A=
ENST00000696272.1:c.413A= ENSP00000512515.1:p.Asp138=
ENST00000696273.1:c.461A= ENSP00000512516.1:p.Asp154=
ENST00000229335.11:c.428A= MANE Select ENSP00000229335.6:p.Asp143=
ENST00000229335.10:c.428A= ENSP00000229335.6:p.Asp143=
ENST00000537228.5:c.428-30A= ENSP00000445691.1:n.428-30A=
ENST00000543081.5:c.423+293A=
ENST00000544516.5:c.153-585A=
ENST00000545512.1:c.424A=
ENST00000545576.1:n.754A=
NM_020661.2:c.428A= , LRG_17t1:c.428A= NP_065712.1:p.Asp143=
XM_011520772.1:c.428-30A= XP_011519074.1:n.428-30A=
XM_011520773.1:c.427+293A= XP_011519075.1:n.427+293A=
NM_001330343.1:c.428-30A= NP_001317272.1:n.428-30A=
NM_020661.3:c.428A= NP_065712.1:p.Asp143=
XM_011520773.2:c.427+293A= XP_011519075.1:n.427+293A=
NM_020661.4:c.428A= MANE Select NP_065712.1:p.Asp143=
NM_001330343.2:c.428-30A= NP_001317272.1:n.428-30A=