Canonical Allele Identifier: CA919018845

Gene: AICDA

Linked Data

• dbSNP Id: rs1565509301
• gnomAD v4: 12-8605142-AACTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8605144_8605147del , CM000674.2:g.8605144_8605147del	GRCh38
NC_000012.11:g.8757740_8757743del , CM000674.1:g.8757740_8757743del	GRCh37
NC_000012.10:g.8649007_8649010del	NCBI36
NG_011588.1:g.12701_12704del , LRG_17:g.12701_12704del

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.427+69_427+72del	ENSP00000445691.1:n.427+69_427+72del
ENST00000543081.6:c.427+69_427+72del	ENSP00000439103.2:n.427+69_427+72del
ENST00000544516.6:c.157-809_157-806del	ENSP00000439538.2:n.157-809_157-806del
ENST00000545576.2:n.605_608del
ENST00000696246.1:c.412+69_412+72del	ENSP00000512504.1:n.412+69_412+72del
ENST00000696271.1:n.616_619del
ENST00000696272.1:c.412+69_412+72del	ENSP00000512515.1:n.412+69_412+72del
ENST00000696273.1:c.460+69_460+72del	ENSP00000512516.1:n.460+69_460+72del
ENST00000229335.11:c.427+69_427+72del MANE Select	ENSP00000229335.6:n.427+69_427+72del
ENST00000229335.10:c.427+69_427+72del	ENSP00000229335.6:n.427+69_427+72del
ENST00000537228.5:c.427+69_427+72del	ENSP00000445691.1:n.427+69_427+72del
ENST00000543081.5:c.423+69_423+72del
ENST00000544516.5:c.153-809_153-806del
ENST00000545512.1:c.423+69_423+72del
ENST00000545576.1:n.530_533del
NM_020661.2:c.427+69_427+72del , LRG_17t1:c.427+69_427+72del	NP_065712.1:n.427+69_427+72del
XM_011520772.1:c.427+69_427+72del	XP_011519074.1:n.427+69_427+72del
XM_011520773.1:c.427+69_427+72del	XP_011519075.1:n.427+69_427+72del
NM_001330343.1:c.427+69_427+72del	NP_001317272.1:n.427+69_427+72del
NM_020661.3:c.427+69_427+72del	NP_065712.1:n.427+69_427+72del
XM_011520773.2:c.427+69_427+72del	XP_011519075.1:n.427+69_427+72del
NM_020661.4:c.427+69_427+72del MANE Select	NP_065712.1:n.427+69_427+72del
NM_001330343.2:c.427+69_427+72del	NP_001317272.1:n.427+69_427+72del