Canonical Allele Identifier: CA2015109659

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604766A= , CM000674.2:g.8604766A=	GRCh38
NC_000012.11:g.8757362A= , CM000674.1:g.8757362A=	GRCh37
NC_000012.10:g.8648629A=	NCBI36
NG_011588.1:g.13081T= , LRG_17:g.13081T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.513+41T=	ENSP00000445691.1:n.513+41T=
ENST00000543081.6:c.428-429T=	ENSP00000439103.2:n.428-429T=
ENST00000544516.6:c.157-429T=	ENSP00000439538.2:n.157-429T=
ENST00000545576.2:n.944+41T=
ENST00000696246.1:c.498+41T=	ENSP00000512504.1:n.498+41T=
ENST00000696271.1:n.955+41T=
ENST00000696272.1:c.528+41T=	ENSP00000512515.1:n.528+41T=
ENST00000696273.1:c.576+41T=	ENSP00000512516.1:n.576+41T=
ENST00000229335.11:c.543+41T= MANE Select	ENSP00000229335.6:n.543+41T=
ENST00000229335.10:c.543+41T=	ENSP00000229335.6:n.543+41T=
ENST00000537228.5:c.513+41T=	ENSP00000445691.1:n.513+41T=
ENST00000543081.5:c.424-429T=
ENST00000544516.5:c.153-429T=
ENST00000545512.1:c.539+41T=
ENST00000545576.1:n.869+41T=
NM_020661.2:c.543+41T= , LRG_17t1:c.543+41T=	NP_065712.1:n.543+41T=
XM_011520772.1:c.513+41T=	XP_011519074.1:n.513+41T=
XM_011520773.1:c.428-429T=	XP_011519075.1:n.428-429T=
NM_001330343.1:c.513+41T=	NP_001317272.1:n.513+41T=
NM_020661.3:c.543+41T=	NP_065712.1:n.543+41T=
XM_011520773.2:c.428-429T=	XP_011519075.1:n.428-429T=
NM_020661.4:c.543+41T= MANE Select	NP_065712.1:n.543+41T=
NM_001330343.2:c.513+41T=	NP_001317272.1:n.513+41T=