Canonical Allele Identifier: CA2575070224
Gene: AICDA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604927_8604928insT , CM000674.2:g.8604927_8604928insT GRCh38
NC_000012.11:g.8757523_8757524insT , CM000674.1:g.8757523_8757524insT GRCh37
NC_000012.10:g.8648790_8648791insT NCBI36
NG_011588.1:g.12919_12920insA , LRG_17:g.12919_12920insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.428-36_428-35insA ENSP00000445691.1:n.428-36_428-35insA
ENST00000543081.6:c.427+287_427+288insA ENSP00000439103.2:n.427+287_427+288insA
ENST00000544516.6:c.157-591_157-590insA ENSP00000439538.2:n.157-591_157-590insA
ENST00000545576.2:n.823_824insA
ENST00000696246.1:c.413-36_413-35insA ENSP00000512504.1:n.413-36_413-35insA
ENST00000696271.1:n.834_835insA
ENST00000696272.1:c.413-6_413-5insA ENSP00000512515.1:n.413-6_413-5insA
ENST00000696273.1:c.461-6_461-5insA ENSP00000512516.1:n.461-6_461-5insA
ENST00000229335.11:c.428-6_428-5insA MANE Select ENSP00000229335.6:n.428-6_428-5insA
ENST00000229335.10:c.428-6_428-5insA ENSP00000229335.6:n.428-6_428-5insA
ENST00000537228.5:c.428-36_428-35insA ENSP00000445691.1:n.428-36_428-35insA
ENST00000543081.5:c.423+287_423+288insA
ENST00000544516.5:c.153-591_153-590insA
ENST00000545512.1:c.424-6_424-5insA
ENST00000545576.1:n.748_749insA
NM_020661.2:c.428-6_428-5insA , LRG_17t1:c.428-6_428-5insA NP_065712.1:n.428-6_428-5insA
XM_011520772.1:c.428-36_428-35insA XP_011519074.1:n.428-36_428-35insA
XM_011520773.1:c.427+287_427+288insA XP_011519075.1:n.427+287_427+288insA
NM_001330343.1:c.428-36_428-35insA NP_001317272.1:n.428-36_428-35insA
NM_020661.3:c.428-6_428-5insA NP_065712.1:n.428-6_428-5insA
XM_011520773.2:c.427+287_427+288insA XP_011519075.1:n.427+287_427+288insA
NM_020661.4:c.428-6_428-5insA MANE Select NP_065712.1:n.428-6_428-5insA
NM_001330343.2:c.428-36_428-35insA NP_001317272.1:n.428-36_428-35insA