Canonical Allele Identifier: CA2015109767

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604884C= , CM000674.2:g.8604884C=	GRCh38
NC_000012.11:g.8757480C= , CM000674.1:g.8757480C=	GRCh37
NC_000012.10:g.8648747C=	NCBI36
NG_011588.1:g.12963G= , LRG_17:g.12963G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.436G=	ENSP00000445691.1:p.Glu146=
ENST00000543081.6:c.427+331G=	ENSP00000439103.2:n.427+331G=
ENST00000544516.6:c.157-547G=	ENSP00000439538.2:n.157-547G=
ENST00000545576.2:n.867G=
ENST00000696246.1:c.421G=	ENSP00000512504.1:p.Glu141=
ENST00000696271.1:n.878G=
ENST00000696272.1:c.451G=	ENSP00000512515.1:p.Glu151=
ENST00000696273.1:c.499G=	ENSP00000512516.1:p.Glu167=
ENST00000229335.11:c.466G= MANE Select	ENSP00000229335.6:p.Glu156=
ENST00000229335.10:c.466G=	ENSP00000229335.6:p.Glu156=
ENST00000537228.5:c.436G=	ENSP00000445691.1:p.Glu146=
ENST00000543081.5:c.423+331G=
ENST00000544516.5:c.153-547G=
ENST00000545512.1:c.462G=
ENST00000545576.1:n.792G=
NM_020661.2:c.466G= , LRG_17t1:c.466G=	NP_065712.1:p.Glu156=
XM_011520772.1:c.436G=	XP_011519074.1:p.Glu146=
XM_011520773.1:c.427+331G=	XP_011519075.1:n.427+331G=
NM_001330343.1:c.436G=	NP_001317272.1:p.Glu146=
NM_020661.3:c.466G=	NP_065712.1:p.Glu156=
XM_011520773.2:c.427+331G=	XP_011519075.1:n.427+331G=
NM_020661.4:c.466G= MANE Select	NP_065712.1:p.Glu156=
NM_001330343.2:c.436G=	NP_001317272.1:p.Glu146=