Canonical Allele Identifier: CA2015109797
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604907C= , CM000674.2:g.8604907C= GRCh38
NC_000012.11:g.8757503C= , CM000674.1:g.8757503C= GRCh37
NC_000012.10:g.8648770C= NCBI36
NG_011588.1:g.12940G= , LRG_17:g.12940G=

Transcript Alleles

HGVS Amino-acid change
ENST00000537228.6:c.428-15G= ENSP00000445691.1:n.428-15G=
ENST00000543081.6:c.427+308G= ENSP00000439103.2:n.427+308G=
ENST00000544516.6:c.157-570G= ENSP00000439538.2:n.157-570G=
ENST00000545576.2:n.844G=
ENST00000696246.1:c.413-15G= ENSP00000512504.1:n.413-15G=
ENST00000696271.1:n.855G=
ENST00000696272.1:c.428G= ENSP00000512515.1:p.Trp143=
ENST00000696273.1:c.476G= ENSP00000512516.1:p.Trp159=
ENST00000229335.11:c.443G= MANE Select ENSP00000229335.6:p.Trp148=
ENST00000229335.10:c.443G= ENSP00000229335.6:p.Trp148=
ENST00000537228.5:c.428-15G= ENSP00000445691.1:n.428-15G=
ENST00000543081.5:c.423+308G=
ENST00000544516.5:c.153-570G=
ENST00000545512.1:c.439G=
ENST00000545576.1:n.769G=
NM_020661.2:c.443G= , LRG_17t1:c.443G= NP_065712.1:p.Trp148=
XM_011520772.1:c.428-15G= XP_011519074.1:n.428-15G=
XM_011520773.1:c.427+308G= XP_011519075.1:n.427+308G=
NM_001330343.1:c.428-15G= NP_001317272.1:n.428-15G=
NM_020661.3:c.443G= NP_065712.1:p.Trp148=
XM_011520773.2:c.427+308G= XP_011519075.1:n.427+308G=
NM_020661.4:c.443G= MANE Select NP_065712.1:p.Trp148=
NM_001330343.2:c.428-15G= NP_001317272.1:n.428-15G=