Canonical Allele Identifier: CA2015111969

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8606950C= , CM000674.2:g.8606950C=	GRCh38
NC_000012.11:g.8759546C= , CM000674.1:g.8759546C=	GRCh37
NC_000012.10:g.8650813C=	NCBI36
NG_011588.1:g.10897G= , LRG_17:g.10897G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.71G=	ENSP00000445691.1:p.Arg24=
ENST00000543081.6:c.71G=	ENSP00000439103.2:p.Arg24=
ENST00000544516.6:c.71G=	ENSP00000439538.2:p.Arg24=
ENST00000545576.2:n.180G=
ENST00000696246.1:c.56G=	ENSP00000512504.1:p.Arg19=
ENST00000696271.1:n.191G=
ENST00000696272.1:c.56G=	ENSP00000512515.1:p.Arg19=
ENST00000696273.1:c.104G=	ENSP00000512516.1:p.Arg35=
ENST00000229335.11:c.71G= MANE Select	ENSP00000229335.6:p.Arg24=
ENST00000229335.10:c.71G=	ENSP00000229335.6:p.Arg24=
ENST00000537228.5:c.71G=	ENSP00000445691.1:p.Arg24=
ENST00000543081.5:c.67G=
ENST00000544516.5:c.67G=
ENST00000545512.1:c.67G=
ENST00000545576.1:n.105G=
NM_020661.2:c.71G= , LRG_17t1:c.71G=	NP_065712.1:p.Arg24=
XM_011520772.1:c.71G=	XP_011519074.1:p.Arg24=
XM_011520773.1:c.71G=	XP_011519075.1:p.Arg24=
NM_001330343.1:c.71G=	NP_001317272.1:p.Arg24=
NM_020661.3:c.71G=	NP_065712.1:p.Arg24=
XM_011520773.2:c.71G=	XP_011519075.1:p.Arg24=
NM_020661.4:c.71G= MANE Select	NP_065712.1:p.Arg24=
NM_001330343.2:c.71G=	NP_001317272.1:p.Arg24=