Canonical Allele Identifier: CA2015110510

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8605375G= , CM000674.2:g.8605375G=	GRCh38
NC_000012.11:g.8757971G= , CM000674.1:g.8757971G=	GRCh37
NC_000012.10:g.8649238G=	NCBI36
NG_011588.1:g.12472C= , LRG_17:g.12472C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.267C=	ENSP00000445691.1:p.Asp89=
ENST00000543081.6:c.267C=	ENSP00000439103.2:p.Asp89=
ENST00000544516.6:c.157-1038C=	ENSP00000439538.2:n.157-1038C=
ENST00000545576.2:n.376C=
ENST00000696246.1:c.252C=	ENSP00000512504.1:p.Asp84=
ENST00000696271.1:n.387C=
ENST00000696272.1:c.252C=	ENSP00000512515.1:p.Asp84=
ENST00000696273.1:c.300C=	ENSP00000512516.1:p.Asp100=
ENST00000229335.11:c.267C= MANE Select	ENSP00000229335.6:p.Asp89=
ENST00000229335.10:c.267C=	ENSP00000229335.6:p.Asp89=
ENST00000537228.5:c.267C=	ENSP00000445691.1:p.Asp89=
ENST00000543081.5:c.263C=
ENST00000544516.5:c.153-1038C=
ENST00000545512.1:c.263C=
ENST00000545576.1:n.301C=
NM_020661.2:c.267C= , LRG_17t1:c.267C=	NP_065712.1:p.Asp89=
XM_011520772.1:c.267C=	XP_011519074.1:p.Asp89=
XM_011520773.1:c.267C=	XP_011519075.1:p.Asp89=
NM_001330343.1:c.267C=	NP_001317272.1:p.Asp89=
NM_020661.3:c.267C=	NP_065712.1:p.Asp89=
XM_011520773.2:c.267C=	XP_011519075.1:p.Asp89=
NM_020661.4:c.267C= MANE Select	NP_065712.1:p.Asp89=
NM_001330343.2:c.267C=	NP_001317272.1:p.Asp89=