Canonical Allele Identifier: CA2015109852

Gene: AICDA

Linked Data

• dbSNP Id: rs1941254159
• gnomAD v4: 12-8604925-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604926del , CM000674.2:g.8604926del	GRCh38
NC_000012.11:g.8757522del , CM000674.1:g.8757522del	GRCh37
NC_000012.10:g.8648789del	NCBI36
NG_011588.1:g.12921del , LRG_17:g.12921del

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.428-34del	ENSP00000445691.1:n.428-34del
ENST00000543081.6:c.427+289del	ENSP00000439103.2:n.427+289del
ENST00000544516.6:c.157-589del	ENSP00000439538.2:n.157-589del
ENST00000545576.2:n.825del
ENST00000696246.1:c.413-34del	ENSP00000512504.1:n.413-34del
ENST00000696271.1:n.836del
ENST00000696272.1:c.413-4del	ENSP00000512515.1:n.413-4del
ENST00000696273.1:c.461-4del	ENSP00000512516.1:n.461-4del
ENST00000229335.11:c.428-4del MANE Select	ENSP00000229335.6:n.428-4del
ENST00000229335.10:c.428-4del	ENSP00000229335.6:n.428-4del
ENST00000537228.5:c.428-34del	ENSP00000445691.1:n.428-34del
ENST00000543081.5:c.423+289del
ENST00000544516.5:c.153-589del
ENST00000545512.1:c.424-4del
ENST00000545576.1:n.750del
NM_020661.2:c.428-4del , LRG_17t1:c.428-4del	NP_065712.1:n.428-4del
XM_011520772.1:c.428-34del	XP_011519074.1:n.428-34del
XM_011520773.1:c.427+289del	XP_011519075.1:n.427+289del
NM_001330343.1:c.428-34del	NP_001317272.1:n.428-34del
NM_020661.3:c.428-4del	NP_065712.1:n.428-4del
XM_011520773.2:c.427+289del	XP_011519075.1:n.427+289del
NM_020661.4:c.428-4del MANE Select	NP_065712.1:n.428-4del
NM_001330343.2:c.428-34del	NP_001317272.1:n.428-34del