Canonical Allele Identifier: CA2015109732

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604833A= , CM000674.2:g.8604833A=	GRCh38
NC_000012.11:g.8757429A= , CM000674.1:g.8757429A=	GRCh37
NC_000012.10:g.8648696A=	NCBI36
NG_011588.1:g.13014T= , LRG_17:g.13014T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.487T=	ENSP00000445691.1:p.Ser163=
ENST00000543081.6:c.427+382T=	ENSP00000439103.2:n.427+382T=
ENST00000544516.6:c.157-496T=	ENSP00000439538.2:n.157-496T=
ENST00000545576.2:n.918T=
ENST00000696246.1:c.472T=	ENSP00000512504.1:p.Ser158=
ENST00000696271.1:n.929T=
ENST00000696272.1:c.502T=	ENSP00000512515.1:p.Ser168=
ENST00000696273.1:c.550T=	ENSP00000512516.1:p.Ser184=
ENST00000229335.11:c.517T= MANE Select	ENSP00000229335.6:p.Ser173=
ENST00000229335.10:c.517T=	ENSP00000229335.6:p.Ser173=
ENST00000537228.5:c.487T=	ENSP00000445691.1:p.Ser163=
ENST00000543081.5:c.423+382T=
ENST00000544516.5:c.153-496T=
ENST00000545512.1:c.513T=
ENST00000545576.1:n.843T=
NM_020661.2:c.517T= , LRG_17t1:c.517T=	NP_065712.1:p.Ser173=
XM_011520772.1:c.487T=	XP_011519074.1:p.Ser163=
XM_011520773.1:c.427+382T=	XP_011519075.1:n.427+382T=
NM_001330343.1:c.487T=	NP_001317272.1:p.Ser163=
NM_020661.3:c.517T=	NP_065712.1:p.Ser173=
XM_011520773.2:c.427+382T=	XP_011519075.1:n.427+382T=
NM_020661.4:c.517T= MANE Select	NP_065712.1:p.Ser173=
NM_001330343.2:c.487T=	NP_001317272.1:p.Ser163=