Canonical Allele Identifier: CA2617496456
Gene: AICDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8605004_8605007dup , CM000674.2:g.8605004_8605007dup GRCh38
NC_000012.11:g.8757600_8757603dup , CM000674.1:g.8757600_8757603dup GRCh37
NC_000012.10:g.8648867_8648870dup NCBI36
NG_011588.1:g.12841_12844dup , LRG_17:g.12841_12844dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.428-114_428-111dup ENSP00000445691.1:n.428-114_428-111dup
ENST00000543081.6:c.427+209_427+212dup ENSP00000439103.2:n.427+209_427+212dup
ENST00000544516.6:c.157-669_157-666dup ENSP00000439538.2:n.157-669_157-666dup
ENST00000545576.2:n.745_748dup
ENST00000696246.1:c.413-114_413-111dup ENSP00000512504.1:n.413-114_413-111dup
ENST00000696271.1:n.756_759dup
ENST00000696272.1:c.413-84_413-81dup ENSP00000512515.1:n.413-84_413-81dup
ENST00000696273.1:c.461-84_461-81dup ENSP00000512516.1:n.461-84_461-81dup
ENST00000229335.11:c.428-84_428-81dup MANE Select ENSP00000229335.6:n.428-84_428-81dup
ENST00000229335.10:c.428-84_428-81dup ENSP00000229335.6:n.428-84_428-81dup
ENST00000537228.5:c.428-114_428-111dup ENSP00000445691.1:n.428-114_428-111dup
ENST00000543081.5:c.423+209_423+212dup
ENST00000544516.5:c.153-669_153-666dup
ENST00000545512.1:c.424-84_424-81dup
ENST00000545576.1:n.670_673dup
NM_020661.2:c.428-84_428-81dup , LRG_17t1:c.428-84_428-81dup NP_065712.1:n.428-84_428-81dup
XM_011520772.1:c.428-114_428-111dup XP_011519074.1:n.428-114_428-111dup
XM_011520773.1:c.427+209_427+212dup XP_011519075.1:n.427+209_427+212dup
NM_001330343.1:c.428-114_428-111dup NP_001317272.1:n.428-114_428-111dup
NM_020661.3:c.428-84_428-81dup NP_065712.1:n.428-84_428-81dup
XM_011520773.2:c.427+209_427+212dup XP_011519075.1:n.427+209_427+212dup
NM_020661.4:c.428-84_428-81dup MANE Select NP_065712.1:n.428-84_428-81dup
NM_001330343.2:c.428-114_428-111dup NP_001317272.1:n.428-114_428-111dup