Canonical Allele Identifier: CA2617496424

Gene: AICDA

Linked Data

• gnomAD v4: 12-8604877-GTTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604881_8604884del , CM000674.2:g.8604881_8604884del	GRCh38
NC_000012.11:g.8757477_8757480del , CM000674.1:g.8757477_8757480del	GRCh37
NC_000012.10:g.8648744_8648747del	NCBI36
NG_011588.1:g.12966_12969del , LRG_17:g.12966_12969del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.439_442del	ENSP00000445691.1:p.Arg147LeufsTer?
ENST00000543081.6:c.427+334_427+337del	ENSP00000439103.2:n.427+334_427+337del
ENST00000544516.6:c.157-544_157-541del	ENSP00000439538.2:n.157-544_157-541del
ENST00000545576.2:n.870_873del
ENST00000696246.1:c.424_427del	ENSP00000512504.1:p.Arg142LeufsTer?
ENST00000696271.1:n.881_884del
ENST00000696272.1:c.454_457del	ENSP00000512515.1:p.Arg152LeufsTer?
ENST00000696273.1:c.502_505del	ENSP00000512516.1:p.Arg168LeufsTer?
ENST00000229335.11:c.469_472del MANE Select	ENSP00000229335.6:p.Arg157LeufsTer?
ENST00000229335.10:c.469_472del	ENSP00000229335.6:p.Arg157LeufsTer?
ENST00000537228.5:c.439_442del	ENSP00000445691.1:p.Arg147LeufsTer?
ENST00000543081.5:c.423+334_423+337del
ENST00000544516.5:c.153-544_153-541del
ENST00000545512.1:c.465_468del
ENST00000545576.1:n.795_798del
NM_020661.2:c.469_472del , LRG_17t1:c.469_472del	NP_065712.1:p.Arg157LeufsTer?
XM_011520772.1:c.439_442del	XP_011519074.1:p.Arg147LeufsTer?
XM_011520773.1:c.427+334_427+337del	XP_011519075.1:n.427+334_427+337del
NM_001330343.1:c.439_442del	NP_001317272.1:p.Arg147LeufsTer?
NM_020661.3:c.469_472del	NP_065712.1:p.Arg157LeufsTer?
XM_011520773.2:c.427+334_427+337del	XP_011519075.1:n.427+334_427+337del
NM_020661.4:c.469_472del MANE Select	NP_065712.1:p.Arg157LeufsTer?
NM_001330343.2:c.439_442del	NP_001317272.1:p.Arg147LeufsTer?