Canonical Allele Identifier: CA2015109793
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604903A= , CM000674.2:g.8604903A= GRCh38
NC_000012.11:g.8757499A= , CM000674.1:g.8757499A= GRCh37
NC_000012.10:g.8648766A= NCBI36
NG_011588.1:g.12944T= , LRG_17:g.12944T=

Transcript Alleles

HGVS Amino-acid change
ENST00000537228.6:c.428-11T= ENSP00000445691.1:n.428-11T=
ENST00000543081.6:c.427+312T= ENSP00000439103.2:n.427+312T=
ENST00000544516.6:c.157-566T= ENSP00000439538.2:n.157-566T=
ENST00000545576.2:n.848T=
ENST00000696246.1:c.413-11T= ENSP00000512504.1:n.413-11T=
ENST00000696271.1:n.859T=
ENST00000696272.1:c.432T= ENSP00000512515.1:p.Asn144=
ENST00000696273.1:c.480T= ENSP00000512516.1:p.Asn160=
ENST00000229335.11:c.447T= MANE Select ENSP00000229335.6:p.Asn149=
ENST00000229335.10:c.447T= ENSP00000229335.6:p.Asn149=
ENST00000537228.5:c.428-11T= ENSP00000445691.1:n.428-11T=
ENST00000543081.5:c.423+312T=
ENST00000544516.5:c.153-566T=
ENST00000545512.1:c.443T=
ENST00000545576.1:n.773T=
NM_020661.2:c.447T= , LRG_17t1:c.447T= NP_065712.1:p.Asn149=
XM_011520772.1:c.428-11T= XP_011519074.1:n.428-11T=
XM_011520773.1:c.427+312T= XP_011519075.1:n.427+312T=
NM_001330343.1:c.428-11T= NP_001317272.1:n.428-11T=
NM_020661.3:c.447T= NP_065712.1:p.Asn149=
XM_011520773.2:c.427+312T= XP_011519075.1:n.427+312T=
NM_020661.4:c.447T= MANE Select NP_065712.1:p.Asn149=
NM_001330343.2:c.428-11T= NP_001317272.1:n.428-11T=