Canonical Allele Identifier: CA2015110564

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8605404A= , CM000674.2:g.8605404A=	GRCh38
NC_000012.11:g.8758000A= , CM000674.1:g.8758000A=	GRCh37
NC_000012.10:g.8649267A=	NCBI36
NG_011588.1:g.12443T= , LRG_17:g.12443T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.238T=	ENSP00000445691.1:p.Trp80=
ENST00000543081.6:c.238T=	ENSP00000439103.2:p.Trp80=
ENST00000544516.6:c.157-1067T=	ENSP00000439538.2:n.157-1067T=
ENST00000545576.2:n.347T=
ENST00000696246.1:c.223T=	ENSP00000512504.1:p.Trp75=
ENST00000696271.1:n.358T=
ENST00000696272.1:c.223T=	ENSP00000512515.1:p.Trp75=
ENST00000696273.1:c.271T=	ENSP00000512516.1:p.Trp91=
ENST00000229335.11:c.238T= MANE Select	ENSP00000229335.6:p.Trp80=
ENST00000229335.10:c.238T=	ENSP00000229335.6:p.Trp80=
ENST00000537228.5:c.238T=	ENSP00000445691.1:p.Trp80=
ENST00000543081.5:c.234T=
ENST00000544516.5:c.153-1067T=
ENST00000545512.1:c.234T=
ENST00000545576.1:n.272T=
NM_020661.2:c.238T= , LRG_17t1:c.238T=	NP_065712.1:p.Trp80=
XM_011520772.1:c.238T=	XP_011519074.1:p.Trp80=
XM_011520773.1:c.238T=	XP_011519075.1:p.Trp80=
NM_001330343.1:c.238T=	NP_001317272.1:p.Trp80=
NM_020661.3:c.238T=	NP_065712.1:p.Trp80=
XM_011520773.2:c.238T=	XP_011519075.1:p.Trp80=
NM_020661.4:c.238T= MANE Select	NP_065712.1:p.Trp80=
NM_001330343.2:c.238T=	NP_001317272.1:p.Trp80=