Canonical Allele Identifier: CA2015109783

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604893C= , CM000674.2:g.8604893C=	GRCh38
NC_000012.11:g.8757489C= , CM000674.1:g.8757489C=	GRCh37
NC_000012.10:g.8648756C=	NCBI36
NG_011588.1:g.12954G= , LRG_17:g.12954G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.428-1G=	ENSP00000445691.1:n.428-1G=
ENST00000543081.6:c.427+322G=	ENSP00000439103.2:n.427+322G=
ENST00000544516.6:c.157-556G=	ENSP00000439538.2:n.157-556G=
ENST00000545576.2:n.858G=
ENST00000696246.1:c.413-1G=	ENSP00000512504.1:n.413-1G=
ENST00000696271.1:n.869G=
ENST00000696272.1:c.442G=	ENSP00000512515.1:p.Glu148=
ENST00000696273.1:c.490G=	ENSP00000512516.1:p.Glu164=
ENST00000229335.11:c.457G= MANE Select	ENSP00000229335.6:p.Glu153=
ENST00000229335.10:c.457G=	ENSP00000229335.6:p.Glu153=
ENST00000537228.5:c.428-1G=	ENSP00000445691.1:n.428-1G=
ENST00000543081.5:c.423+322G=
ENST00000544516.5:c.153-556G=
ENST00000545512.1:c.453G=
ENST00000545576.1:n.783G=
NM_020661.2:c.457G= , LRG_17t1:c.457G=	NP_065712.1:p.Glu153=
XM_011520772.1:c.428-1G=	XP_011519074.1:n.428-1G=
XM_011520773.1:c.427+322G=	XP_011519075.1:n.427+322G=
NM_001330343.1:c.428-1G=	NP_001317272.1:n.428-1G=
NM_020661.3:c.457G=	NP_065712.1:p.Glu153=
XM_011520773.2:c.427+322G=	XP_011519075.1:n.427+322G=
NM_020661.4:c.457G= MANE Select	NP_065712.1:p.Glu153=
NM_001330343.2:c.428-1G=	NP_001317272.1:n.428-1G=