Canonical Allele Identifier: CA2575070274

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8606856A>T , CM000674.2:g.8606856A>T	GRCh38
NC_000012.11:g.8759452A>T , CM000674.1:g.8759452A>T	GRCh37
NC_000012.10:g.8650719A>T	NCBI36
NG_011588.1:g.10991T>A , LRG_17:g.10991T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.156+9T>A	ENSP00000445691.1:n.156+9T>A
ENST00000543081.6:c.156+9T>A	ENSP00000439103.2:n.156+9T>A
ENST00000544516.6:c.156+9T>A	ENSP00000439538.2:n.156+9T>A
ENST00000545576.2:n.265+9T>A
ENST00000696246.1:c.141+9T>A	ENSP00000512504.1:n.141+9T>A
ENST00000696271.1:n.276+9T>A
ENST00000696272.1:c.141+9T>A	ENSP00000512515.1:n.141+9T>A
ENST00000696273.1:c.189+9T>A	ENSP00000512516.1:n.189+9T>A
ENST00000229335.11:c.156+9T>A MANE Select	ENSP00000229335.6:n.156+9T>A
ENST00000229335.10:c.156+9T>A	ENSP00000229335.6:n.156+9T>A
ENST00000537228.5:c.156+9T>A	ENSP00000445691.1:n.156+9T>A
ENST00000543081.5:c.152+9T>A
ENST00000544516.5:c.152+9T>A
ENST00000545512.1:c.152+9T>A
ENST00000545576.1:n.190+9T>A
NM_020661.2:c.156+9T>A , LRG_17t1:c.156+9T>A	NP_065712.1:n.156+9T>A
XM_011520772.1:c.156+9T>A	XP_011519074.1:n.156+9T>A
XM_011520773.1:c.156+9T>A	XP_011519075.1:n.156+9T>A
NM_001330343.1:c.156+9T>A	NP_001317272.1:n.156+9T>A
NM_020661.3:c.156+9T>A	NP_065712.1:n.156+9T>A
XM_011520773.2:c.156+9T>A	XP_011519075.1:n.156+9T>A
NM_020661.4:c.156+9T>A MANE Select	NP_065712.1:n.156+9T>A
NM_001330343.2:c.156+9T>A	NP_001317272.1:n.156+9T>A