Canonical Allele Identifier: CA2015109558

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604645G= , CM000674.2:g.8604645G=	GRCh38
NC_000012.11:g.8757241G= , CM000674.1:g.8757241G=	GRCh37
NC_000012.10:g.8648508G=	NCBI36
NG_011588.1:g.13202C= , LRG_17:g.13202C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.513+162C=	ENSP00000445691.1:n.513+162C=
ENST00000543081.6:c.428-308C=	ENSP00000439103.2:n.428-308C=
ENST00000544516.6:c.157-308C=	ENSP00000439538.2:n.157-308C=
ENST00000545576.2:n.944+162C=
ENST00000696246.1:c.498+162C=	ENSP00000512504.1:n.498+162C=
ENST00000696271.1:n.955+162C=
ENST00000696272.1:c.528+162C=	ENSP00000512515.1:n.528+162C=
ENST00000696273.1:c.576+162C=	ENSP00000512516.1:n.576+162C=
ENST00000229335.11:c.543+162C= MANE Select	ENSP00000229335.6:n.543+162C=
ENST00000229335.10:c.543+162C=	ENSP00000229335.6:n.543+162C=
ENST00000537228.5:c.513+162C=	ENSP00000445691.1:n.513+162C=
ENST00000543081.5:c.424-308C=
ENST00000544516.5:c.153-308C=
ENST00000545512.1:c.539+162C=
ENST00000545576.1:n.869+162C=
NM_020661.2:c.543+162C= , LRG_17t1:c.543+162C=	NP_065712.1:n.543+162C=
XM_011520772.1:c.513+162C=	XP_011519074.1:n.513+162C=
XM_011520773.1:c.428-308C=	XP_011519075.1:n.428-308C=
NM_001330343.1:c.513+162C=	NP_001317272.1:n.513+162C=
NM_020661.3:c.543+162C=	NP_065712.1:n.543+162C=
XM_011520773.2:c.428-308C=	XP_011519075.1:n.428-308C=
NM_020661.4:c.543+162C= MANE Select	NP_065712.1:n.543+162C=
NM_001330343.2:c.513+162C=	NP_001317272.1:n.513+162C=