Canonical Allele Identifier: CA2015109875
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604927A= , CM000674.2:g.8604927A= GRCh38
NC_000012.11:g.8757523A= , CM000674.1:g.8757523A= GRCh37
NC_000012.10:g.8648790A= NCBI36
NG_011588.1:g.12920T= , LRG_17:g.12920T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.428-35T= ENSP00000445691.1:n.428-35T=
ENST00000543081.6:c.427+288T= ENSP00000439103.2:n.427+288T=
ENST00000544516.6:c.157-590T= ENSP00000439538.2:n.157-590T=
ENST00000545576.2:n.824T=
ENST00000696246.1:c.413-35T= ENSP00000512504.1:n.413-35T=
ENST00000696271.1:n.835T=
ENST00000696272.1:c.413-5T= ENSP00000512515.1:n.413-5T=
ENST00000696273.1:c.461-5T= ENSP00000512516.1:n.461-5T=
ENST00000229335.11:c.428-5T= MANE Select ENSP00000229335.6:n.428-5T=
ENST00000229335.10:c.428-5T= ENSP00000229335.6:n.428-5T=
ENST00000537228.5:c.428-35T= ENSP00000445691.1:n.428-35T=
ENST00000543081.5:c.423+288T=
ENST00000544516.5:c.153-590T=
ENST00000545512.1:c.424-5T=
ENST00000545576.1:n.749T=
NM_020661.2:c.428-5T= , LRG_17t1:c.428-5T= NP_065712.1:n.428-5T=
XM_011520772.1:c.428-35T= XP_011519074.1:n.428-35T=
XM_011520773.1:c.427+288T= XP_011519075.1:n.427+288T=
NM_001330343.1:c.428-35T= NP_001317272.1:n.428-35T=
NM_020661.3:c.428-5T= NP_065712.1:n.428-5T=
XM_011520773.2:c.427+288T= XP_011519075.1:n.427+288T=
NM_020661.4:c.428-5T= MANE Select NP_065712.1:n.428-5T=
NM_001330343.2:c.428-35T= NP_001317272.1:n.428-35T=