Canonical Allele Identifier: CA654242796

Gene: AICDA

Linked Data

• COSMIC: COSN20081642

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604467_8604468insT , CM000674.2:g.8604467_8604468insT	GRCh38
NC_000012.11:g.8757063_8757064insT , CM000674.1:g.8757063_8757064insT	GRCh37
NC_000012.10:g.8648330_8648331insT	NCBI36
NG_011588.1:g.13379_13380insA , LRG_17:g.13379_13380insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.514-131_514-130insA	ENSP00000445691.1:n.514-131_514-130insA
ENST00000543081.6:c.428-131_428-130insA	ENSP00000439103.2:n.428-131_428-130insA
ENST00000544516.6:c.157-131_157-130insA	ENSP00000439538.2:n.157-131_157-130insA
ENST00000545576.2:n.945-131_945-130insA
ENST00000696246.1:c.499-131_499-130insA	ENSP00000512504.1:n.499-131_499-130insA
ENST00000696271.1:n.956-131_956-130insA
ENST00000696272.1:c.529-131_529-130insA	ENSP00000512515.1:n.529-131_529-130insA
ENST00000696273.1:c.577-131_577-130insA	ENSP00000512516.1:n.577-131_577-130insA
ENST00000229335.11:c.544-131_544-130insA MANE Select	ENSP00000229335.6:n.544-131_544-130insA
ENST00000229335.10:c.544-131_544-130insA	ENSP00000229335.6:n.544-131_544-130insA
ENST00000537228.5:c.514-131_514-130insA	ENSP00000445691.1:n.514-131_514-130insA
ENST00000543081.5:c.424-131_424-130insA
ENST00000544516.5:c.153-131_153-130insA
ENST00000545512.1:c.540-131_540-130insA
ENST00000545576.1:n.870-131_870-130insA
NM_020661.2:c.544-131_544-130insA , LRG_17t1:c.544-131_544-130insA	NP_065712.1:n.544-131_544-130insA
XM_011520772.1:c.514-131_514-130insA	XP_011519074.1:n.514-131_514-130insA
XM_011520773.1:c.428-131_428-130insA	XP_011519075.1:n.428-131_428-130insA
NM_001330343.1:c.514-131_514-130insA	NP_001317272.1:n.514-131_514-130insA
NM_020661.3:c.544-131_544-130insA	NP_065712.1:n.544-131_544-130insA
XM_011520773.2:c.428-131_428-130insA	XP_011519075.1:n.428-131_428-130insA
NM_020661.4:c.544-131_544-130insA MANE Select	NP_065712.1:n.544-131_544-130insA
NM_001330343.2:c.514-131_514-130insA	NP_001317272.1:n.514-131_514-130insA