Canonical Allele Identifier: CA2015109668
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604773_8604775delinsGAA , CM000674.2:g.8604773_8604775delinsGAA GRCh38
NC_000012.11:g.8757369_8757371delinsGAA , CM000674.1:g.8757369_8757371delinsGAA GRCh37
NC_000012.10:g.8648636_8648638delinsGAA NCBI36
NG_011588.1:g.13072_13074delinsTTC , LRG_17:g.13072_13074delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.513+32_513+34delinsTTC ENSP00000445691.1:n.513+32_513+34delinsTTC
ENST00000543081.6:c.428-438_428-436delinsTTC ENSP00000439103.2:n.428-438_428-436delinsTTC
ENST00000544516.6:c.157-438_157-436delinsTTC ENSP00000439538.2:n.157-438_157-436delinsTTC
ENST00000545576.2:n.944+32_944+34delinsTTC
ENST00000696246.1:c.498+32_498+34delinsTTC ENSP00000512504.1:n.498+32_498+34delinsTTC
ENST00000696271.1:n.955+32_955+34delinsTTC
ENST00000696272.1:c.528+32_528+34delinsTTC ENSP00000512515.1:n.528+32_528+34delinsTTC
ENST00000696273.1:c.576+32_576+34delinsTTC ENSP00000512516.1:n.576+32_576+34delinsTTC
ENST00000229335.11:c.543+32_543+34delinsTTC MANE Select ENSP00000229335.6:n.543+32_543+34delinsTTC
ENST00000229335.10:c.543+32_543+34delinsTTC ENSP00000229335.6:n.543+32_543+34delinsTTC
ENST00000537228.5:c.513+32_513+34delinsTTC ENSP00000445691.1:n.513+32_513+34delinsTTC
ENST00000543081.5:c.424-438_424-436delinsTTC
ENST00000544516.5:c.153-438_153-436delinsTTC
ENST00000545512.1:c.539+32_539+34delinsTTC
ENST00000545576.1:n.869+32_869+34delinsTTC
NM_020661.2:c.543+32_543+34delinsTTC , LRG_17t1:c.543+32_543+34delinsTTC NP_065712.1:n.543+32_543+34delinsTTC
XM_011520772.1:c.513+32_513+34delinsTTC XP_011519074.1:n.513+32_513+34delinsTTC
XM_011520773.1:c.428-438_428-436delinsTTC XP_011519075.1:n.428-438_428-436delinsTTC
NM_001330343.1:c.513+32_513+34delinsTTC NP_001317272.1:n.513+32_513+34delinsTTC
NM_020661.3:c.543+32_543+34delinsTTC NP_065712.1:n.543+32_543+34delinsTTC
XM_011520773.2:c.428-438_428-436delinsTTC XP_011519075.1:n.428-438_428-436delinsTTC
NM_020661.4:c.543+32_543+34delinsTTC MANE Select NP_065712.1:n.543+32_543+34delinsTTC
NM_001330343.2:c.513+32_513+34delinsTTC NP_001317272.1:n.513+32_513+34delinsTTC