Canonical Allele Identifier: CA2015109233
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604415T= , CM000674.2:g.8604415T= GRCh38
NC_000012.11:g.8757011T= , CM000674.1:g.8757011T= GRCh37
NC_000012.10:g.8648278T= NCBI36
NG_011588.1:g.13432A= , LRG_17:g.13432A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-78A= ENSP00000445691.1:n.514-78A=
ENST00000543081.6:c.428-78A= ENSP00000439103.2:n.428-78A=
ENST00000544516.6:c.157-78A= ENSP00000439538.2:n.157-78A=
ENST00000545576.2:n.945-78A=
ENST00000696246.1:c.499-78A= ENSP00000512504.1:n.499-78A=
ENST00000696271.1:n.956-78A=
ENST00000696272.1:c.529-78A= ENSP00000512515.1:n.529-78A=
ENST00000696273.1:c.577-78A= ENSP00000512516.1:n.577-78A=
ENST00000229335.11:c.544-78A= MANE Select ENSP00000229335.6:n.544-78A=
ENST00000229335.10:c.544-78A= ENSP00000229335.6:n.544-78A=
ENST00000537228.5:c.514-78A= ENSP00000445691.1:n.514-78A=
ENST00000543081.5:c.424-78A=
ENST00000544516.5:c.153-78A=
ENST00000545512.1:c.540-78A=
ENST00000545576.1:n.870-78A=
NM_020661.2:c.544-78A= , LRG_17t1:c.544-78A= NP_065712.1:n.544-78A=
XM_011520772.1:c.514-78A= XP_011519074.1:n.514-78A=
XM_011520773.1:c.428-78A= XP_011519075.1:n.428-78A=
NM_001330343.1:c.514-78A= NP_001317272.1:n.514-78A=
NM_020661.3:c.544-78A= NP_065712.1:n.544-78A=
XM_011520773.2:c.428-78A= XP_011519075.1:n.428-78A=
NM_020661.4:c.544-78A= MANE Select NP_065712.1:n.544-78A=
NM_001330343.2:c.514-78A= NP_001317272.1:n.514-78A=