Canonical Allele Identifier: CA2015109552

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604639C= , CM000674.2:g.8604639C=	GRCh38
NC_000012.11:g.8757235C= , CM000674.1:g.8757235C=	GRCh37
NC_000012.10:g.8648502C=	NCBI36
NG_011588.1:g.13208G= , LRG_17:g.13208G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.513+168G=	ENSP00000445691.1:n.513+168G=
ENST00000543081.6:c.428-302G=	ENSP00000439103.2:n.428-302G=
ENST00000544516.6:c.157-302G=	ENSP00000439538.2:n.157-302G=
ENST00000545576.2:n.944+168G=
ENST00000696246.1:c.498+168G=	ENSP00000512504.1:n.498+168G=
ENST00000696271.1:n.955+168G=
ENST00000696272.1:c.528+168G=	ENSP00000512515.1:n.528+168G=
ENST00000696273.1:c.576+168G=	ENSP00000512516.1:n.576+168G=
ENST00000229335.11:c.543+168G= MANE Select	ENSP00000229335.6:n.543+168G=
ENST00000229335.10:c.543+168G=	ENSP00000229335.6:n.543+168G=
ENST00000537228.5:c.513+168G=	ENSP00000445691.1:n.513+168G=
ENST00000543081.5:c.424-302G=
ENST00000544516.5:c.153-302G=
ENST00000545512.1:c.539+168G=
ENST00000545576.1:n.869+168G=
NM_020661.2:c.543+168G= , LRG_17t1:c.543+168G=	NP_065712.1:n.543+168G=
XM_011520772.1:c.513+168G=	XP_011519074.1:n.513+168G=
XM_011520773.1:c.428-302G=	XP_011519075.1:n.428-302G=
NM_001330343.1:c.513+168G=	NP_001317272.1:n.513+168G=
NM_020661.3:c.543+168G=	NP_065712.1:n.543+168G=
XM_011520773.2:c.428-302G=	XP_011519075.1:n.428-302G=
NM_020661.4:c.543+168G= MANE Select	NP_065712.1:n.543+168G=
NM_001330343.2:c.513+168G=	NP_001317272.1:n.513+168G=