Canonical Allele Identifier: CA2015110101
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8605129G= , CM000674.2:g.8605129G= GRCh38
NC_000012.11:g.8757725G= , CM000674.1:g.8757725G= GRCh37
NC_000012.10:g.8648992G= NCBI36
NG_011588.1:g.12718C= , LRG_17:g.12718C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.427+86C= ENSP00000445691.1:n.427+86C=
ENST00000543081.6:c.427+86C= ENSP00000439103.2:n.427+86C=
ENST00000544516.6:c.157-792C= ENSP00000439538.2:n.157-792C=
ENST00000545576.2:n.622C=
ENST00000696246.1:c.412+86C= ENSP00000512504.1:n.412+86C=
ENST00000696271.1:n.633C=
ENST00000696272.1:c.412+86C= ENSP00000512515.1:n.412+86C=
ENST00000696273.1:c.460+86C= ENSP00000512516.1:n.460+86C=
ENST00000229335.11:c.427+86C= MANE Select ENSP00000229335.6:n.427+86C=
ENST00000229335.10:c.427+86C= ENSP00000229335.6:n.427+86C=
ENST00000537228.5:c.427+86C= ENSP00000445691.1:n.427+86C=
ENST00000543081.5:c.423+86C=
ENST00000544516.5:c.153-792C=
ENST00000545512.1:c.423+86C=
ENST00000545576.1:n.547C=
NM_020661.2:c.427+86C= , LRG_17t1:c.427+86C= NP_065712.1:n.427+86C=
XM_011520772.1:c.427+86C= XP_011519074.1:n.427+86C=
XM_011520773.1:c.427+86C= XP_011519075.1:n.427+86C=
NM_001330343.1:c.427+86C= NP_001317272.1:n.427+86C=
NM_020661.3:c.427+86C= NP_065712.1:n.427+86C=
XM_011520773.2:c.427+86C= XP_011519075.1:n.427+86C=
NM_020661.4:c.427+86C= MANE Select NP_065712.1:n.427+86C=
NM_001330343.2:c.427+86C= NP_001317272.1:n.427+86C=