Canonical Allele Identifier: CA2617496760

Gene: AICDA

Linked Data

• gnomAD v4: 12-8606857-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8606857A>G , CM000674.2:g.8606857A>G	GRCh38
NC_000012.11:g.8759453A>G , CM000674.1:g.8759453A>G	GRCh37
NC_000012.10:g.8650720A>G	NCBI36
NG_011588.1:g.10990T>C , LRG_17:g.10990T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.156+8T>C	ENSP00000445691.1:n.156+8T>C
ENST00000543081.6:c.156+8T>C	ENSP00000439103.2:n.156+8T>C
ENST00000544516.6:c.156+8T>C	ENSP00000439538.2:n.156+8T>C
ENST00000545576.2:n.265+8T>C
ENST00000696246.1:c.141+8T>C	ENSP00000512504.1:n.141+8T>C
ENST00000696271.1:n.276+8T>C
ENST00000696272.1:c.141+8T>C	ENSP00000512515.1:n.141+8T>C
ENST00000696273.1:c.189+8T>C	ENSP00000512516.1:n.189+8T>C
ENST00000229335.11:c.156+8T>C MANE Select	ENSP00000229335.6:n.156+8T>C
ENST00000229335.10:c.156+8T>C	ENSP00000229335.6:n.156+8T>C
ENST00000537228.5:c.156+8T>C	ENSP00000445691.1:n.156+8T>C
ENST00000543081.5:c.152+8T>C
ENST00000544516.5:c.152+8T>C
ENST00000545512.1:c.152+8T>C
ENST00000545576.1:n.190+8T>C
NM_020661.2:c.156+8T>C , LRG_17t1:c.156+8T>C	NP_065712.1:n.156+8T>C
XM_011520772.1:c.156+8T>C	XP_011519074.1:n.156+8T>C
XM_011520773.1:c.156+8T>C	XP_011519075.1:n.156+8T>C
NM_001330343.1:c.156+8T>C	NP_001317272.1:n.156+8T>C
NM_020661.3:c.156+8T>C	NP_065712.1:n.156+8T>C
XM_011520773.2:c.156+8T>C	XP_011519075.1:n.156+8T>C
NM_020661.4:c.156+8T>C MANE Select	NP_065712.1:n.156+8T>C
NM_001330343.2:c.156+8T>C	NP_001317272.1:n.156+8T>C