Canonical Allele Identifier: CA692859058
Gene: AICDA HGNC NCBI

Linked Data

dbSNP Id: rs1466918379

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604605_8604609del , CM000674.2:g.8604605_8604609del GRCh38
NC_000012.11:g.8757201_8757205del , CM000674.1:g.8757201_8757205del GRCh37
NC_000012.10:g.8648468_8648472del NCBI36
NG_011588.1:g.13242_13246del , LRG_17:g.13242_13246del

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.513+202_513+206del ENSP00000445691.1:n.513+202_513+206del
ENST00000543081.6:c.428-268_428-264del ENSP00000439103.2:n.428-268_428-264del
ENST00000544516.6:c.157-268_157-264del ENSP00000439538.2:n.157-268_157-264del
ENST00000545576.2:n.944+202_944+206del
ENST00000696246.1:c.498+202_498+206del ENSP00000512504.1:n.498+202_498+206del
ENST00000696271.1:n.955+202_955+206del
ENST00000696272.1:c.528+202_528+206del ENSP00000512515.1:n.528+202_528+206del
ENST00000696273.1:c.576+202_576+206del ENSP00000512516.1:n.576+202_576+206del
ENST00000229335.11:c.543+202_543+206del MANE Select ENSP00000229335.6:n.543+202_543+206del
ENST00000229335.10:c.543+202_543+206del ENSP00000229335.6:n.543+202_543+206del
ENST00000537228.5:c.513+202_513+206del ENSP00000445691.1:n.513+202_513+206del
ENST00000543081.5:c.424-268_424-264del
ENST00000544516.5:c.153-268_153-264del
ENST00000545512.1:c.539+202_539+206del
ENST00000545576.1:n.869+202_869+206del
NM_020661.2:c.543+202_543+206del , LRG_17t1:c.543+202_543+206del NP_065712.1:n.543+202_543+206del
XM_011520772.1:c.513+202_513+206del XP_011519074.1:n.513+202_513+206del
XM_011520773.1:c.428-268_428-264del XP_011519075.1:n.428-268_428-264del
NM_001330343.1:c.513+202_513+206del NP_001317272.1:n.513+202_513+206del
NM_020661.3:c.543+202_543+206del NP_065712.1:n.543+202_543+206del
XM_011520773.2:c.428-268_428-264del XP_011519075.1:n.428-268_428-264del
NM_020661.4:c.543+202_543+206del MANE Select NP_065712.1:n.543+202_543+206del
NM_001330343.2:c.513+202_513+206del NP_001317272.1:n.513+202_513+206del