Canonical Allele Identifier: CA944537500
Gene: AICDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604494_8604495insG , CM000674.2:g.8604494_8604495insG GRCh38
NC_000012.11:g.8757090_8757091insG , CM000674.1:g.8757090_8757091insG GRCh37
NC_000012.10:g.8648357_8648358insG NCBI36
NG_011588.1:g.13352_13353insC , LRG_17:g.13352_13353insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-158_514-157insC ENSP00000445691.1:n.514-158_514-157insC
ENST00000543081.6:c.428-158_428-157insC ENSP00000439103.2:n.428-158_428-157insC
ENST00000544516.6:c.157-158_157-157insC ENSP00000439538.2:n.157-158_157-157insC
ENST00000545576.2:n.945-158_945-157insC
ENST00000696246.1:c.499-158_499-157insC ENSP00000512504.1:n.499-158_499-157insC
ENST00000696271.1:n.956-158_956-157insC
ENST00000696272.1:c.529-158_529-157insC ENSP00000512515.1:n.529-158_529-157insC
ENST00000696273.1:c.577-158_577-157insC ENSP00000512516.1:n.577-158_577-157insC
ENST00000229335.11:c.544-158_544-157insC MANE Select ENSP00000229335.6:n.544-158_544-157insC
ENST00000229335.10:c.544-158_544-157insC ENSP00000229335.6:n.544-158_544-157insC
ENST00000537228.5:c.514-158_514-157insC ENSP00000445691.1:n.514-158_514-157insC
ENST00000543081.5:c.424-158_424-157insC
ENST00000544516.5:c.153-158_153-157insC
ENST00000545512.1:c.540-158_540-157insC
ENST00000545576.1:n.870-158_870-157insC
NM_020661.2:c.544-158_544-157insC , LRG_17t1:c.544-158_544-157insC NP_065712.1:n.544-158_544-157insC
XM_011520772.1:c.514-158_514-157insC XP_011519074.1:n.514-158_514-157insC
XM_011520773.1:c.428-158_428-157insC XP_011519075.1:n.428-158_428-157insC
NM_001330343.1:c.514-158_514-157insC NP_001317272.1:n.514-158_514-157insC
NM_020661.3:c.544-158_544-157insC NP_065712.1:n.544-158_544-157insC
XM_011520773.2:c.428-158_428-157insC XP_011519075.1:n.428-158_428-157insC
NM_020661.4:c.544-158_544-157insC MANE Select NP_065712.1:n.544-158_544-157insC
NM_001330343.2:c.514-158_514-157insC NP_001317272.1:n.514-158_514-157insC