Canonical Allele Identifier: CA603490262

Gene: AICDA

Linked Data

• gnomAD v2: 12-8757519-C-CT
• gnomAD v4: 12-8604923-C-CT
• MyVariant Identifiers: chr12:g.8757519_8757520insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604925dup , CM000674.2:g.8604925dup	GRCh38
NC_000012.11:g.8757521dup , CM000674.1:g.8757521dup	GRCh37
NC_000012.10:g.8648788dup	NCBI36
NG_011588.1:g.12923dup , LRG_17:g.12923dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.428-32dup	ENSP00000445691.1:n.428-32dup
ENST00000543081.6:c.427+291dup	ENSP00000439103.2:n.427+291dup
ENST00000544516.6:c.157-587dup	ENSP00000439538.2:n.157-587dup
ENST00000545576.2:n.827dup
ENST00000696246.1:c.413-32dup	ENSP00000512504.1:n.413-32dup
ENST00000696271.1:n.838dup
ENST00000696272.1:c.413-2dup	ENSP00000512515.1:n.413-2dup
ENST00000696273.1:c.461-2dup	ENSP00000512516.1:n.461-2dup
ENST00000229335.11:c.428-2dup MANE Select	ENSP00000229335.6:n.428-2dup
ENST00000229335.10:c.428-2dup	ENSP00000229335.6:n.428-2dup
ENST00000537228.5:c.428-32dup	ENSP00000445691.1:n.428-32dup
ENST00000543081.5:c.423+291dup
ENST00000544516.5:c.153-587dup
ENST00000545512.1:c.424-2dup
ENST00000545576.1:n.752dup
NM_020661.2:c.428-2dup , LRG_17t1:c.428-2dup	NP_065712.1:n.428-2dup
XM_011520772.1:c.428-32dup	XP_011519074.1:n.428-32dup
XM_011520773.1:c.427+291dup	XP_011519075.1:n.427+291dup
NM_001330343.1:c.428-32dup	NP_001317272.1:n.428-32dup
NM_020661.3:c.428-2dup	NP_065712.1:n.428-2dup
XM_011520773.2:c.427+291dup	XP_011519075.1:n.427+291dup
NM_020661.4:c.428-2dup MANE Select	NP_065712.1:n.428-2dup
NM_001330343.2:c.428-32dup	NP_001317272.1:n.428-32dup