Canonical Allele Identifier: CA2015109942

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604958A= , CM000674.2:g.8604958A=	GRCh38
NC_000012.11:g.8757554A= , CM000674.1:g.8757554A=	GRCh37
NC_000012.10:g.8648821A=	NCBI36
NG_011588.1:g.12889T= , LRG_17:g.12889T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.428-66T=	ENSP00000445691.1:n.428-66T=
ENST00000543081.6:c.427+257T=	ENSP00000439103.2:n.427+257T=
ENST00000544516.6:c.157-621T=	ENSP00000439538.2:n.157-621T=
ENST00000545576.2:n.793T=
ENST00000696246.1:c.413-66T=	ENSP00000512504.1:n.413-66T=
ENST00000696271.1:n.804T=
ENST00000696272.1:c.413-36T=	ENSP00000512515.1:n.413-36T=
ENST00000696273.1:c.461-36T=	ENSP00000512516.1:n.461-36T=
ENST00000229335.11:c.428-36T= MANE Select	ENSP00000229335.6:n.428-36T=
ENST00000229335.10:c.428-36T=	ENSP00000229335.6:n.428-36T=
ENST00000537228.5:c.428-66T=	ENSP00000445691.1:n.428-66T=
ENST00000543081.5:c.423+257T=
ENST00000544516.5:c.153-621T=
ENST00000545512.1:c.424-36T=
ENST00000545576.1:n.718T=
NM_020661.2:c.428-36T= , LRG_17t1:c.428-36T=	NP_065712.1:n.428-36T=
XM_011520772.1:c.428-66T=	XP_011519074.1:n.428-66T=
XM_011520773.1:c.427+257T=	XP_011519075.1:n.427+257T=
NM_001330343.1:c.428-66T=	NP_001317272.1:n.428-66T=
NM_020661.3:c.428-36T=	NP_065712.1:n.428-36T=
XM_011520773.2:c.427+257T=	XP_011519075.1:n.427+257T=
NM_020661.4:c.428-36T= MANE Select	NP_065712.1:n.428-36T=
NM_001330343.2:c.428-66T=	NP_001317272.1:n.428-66T=