Canonical Allele Identifier: CA2015109698
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604802C= , CM000674.2:g.8604802C= GRCh38
NC_000012.11:g.8757398C= , CM000674.1:g.8757398C= GRCh37
NC_000012.10:g.8648665C= NCBI36
NG_011588.1:g.13045G= , LRG_17:g.13045G=

Transcript Alleles

HGVS Amino-acid change
ENST00000537228.6:c.513+5G= ENSP00000445691.1:n.513+5G=
ENST00000543081.6:c.427+413G= ENSP00000439103.2:n.427+413G=
ENST00000544516.6:c.157-465G= ENSP00000439538.2:n.157-465G=
ENST00000545576.2:n.944+5G=
ENST00000696246.1:c.498+5G= ENSP00000512504.1:n.498+5G=
ENST00000696271.1:n.955+5G=
ENST00000696272.1:c.528+5G= ENSP00000512515.1:n.528+5G=
ENST00000696273.1:c.576+5G= ENSP00000512516.1:n.576+5G=
ENST00000229335.11:c.543+5G= MANE Select ENSP00000229335.6:n.543+5G=
ENST00000229335.10:c.543+5G= ENSP00000229335.6:n.543+5G=
ENST00000537228.5:c.513+5G= ENSP00000445691.1:n.513+5G=
ENST00000543081.5:c.423+413G=
ENST00000544516.5:c.153-465G=
ENST00000545512.1:c.539+5G=
ENST00000545576.1:n.869+5G=
NM_020661.2:c.543+5G= , LRG_17t1:c.543+5G= NP_065712.1:n.543+5G=
XM_011520772.1:c.513+5G= XP_011519074.1:n.513+5G=
XM_011520773.1:c.427+413G= XP_011519075.1:n.427+413G=
NM_001330343.1:c.513+5G= NP_001317272.1:n.513+5G=
NM_020661.3:c.543+5G= NP_065712.1:n.543+5G=
XM_011520773.2:c.427+413G= XP_011519075.1:n.427+413G=
NM_020661.4:c.543+5G= MANE Select NP_065712.1:n.543+5G=
NM_001330343.2:c.513+5G= NP_001317272.1:n.513+5G=