Canonical Allele Identifier: CA2015109711

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604817C= , CM000674.2:g.8604817C=	GRCh38
NC_000012.11:g.8757413C= , CM000674.1:g.8757413C=	GRCh37
NC_000012.10:g.8648680C=	NCBI36
NG_011588.1:g.13030G= , LRG_17:g.13030G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.503G=	ENSP00000445691.1:p.Arg168=
ENST00000543081.6:c.427+398G=	ENSP00000439103.2:n.427+398G=
ENST00000544516.6:c.157-480G=	ENSP00000439538.2:n.157-480G=
ENST00000545576.2:n.934G=
ENST00000696246.1:c.488G=	ENSP00000512504.1:p.Arg163=
ENST00000696271.1:n.945G=
ENST00000696272.1:c.518G=	ENSP00000512515.1:p.Arg173=
ENST00000696273.1:c.566G=	ENSP00000512516.1:p.Arg189=
ENST00000229335.11:c.533G= MANE Select	ENSP00000229335.6:p.Arg178=
ENST00000229335.10:c.533G=	ENSP00000229335.6:p.Arg178=
ENST00000537228.5:c.503G=	ENSP00000445691.1:p.Arg168=
ENST00000543081.5:c.423+398G=
ENST00000544516.5:c.153-480G=
ENST00000545512.1:c.529G=
ENST00000545576.1:n.859G=
NM_020661.2:c.533G= , LRG_17t1:c.533G=	NP_065712.1:p.Arg178=
XM_011520772.1:c.503G=	XP_011519074.1:p.Arg168=
XM_011520773.1:c.427+398G=	XP_011519075.1:n.427+398G=
NM_001330343.1:c.503G=	NP_001317272.1:p.Arg168=
NM_020661.3:c.533G=	NP_065712.1:p.Arg178=
XM_011520773.2:c.427+398G=	XP_011519075.1:n.427+398G=
NM_020661.4:c.533G= MANE Select	NP_065712.1:p.Arg178=
NM_001330343.2:c.503G=	NP_001317272.1:p.Arg168=