Canonical Allele Identifier: CA478291482

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757436A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604840A>C , CM000674.2:g.8604840A>C	GRCh38
NC_000012.11:g.8757436A>C , CM000674.1:g.8757436A>C	GRCh37
NC_000012.10:g.8648703A>C	NCBI36
NG_011588.1:g.13007T>G , LRG_17:g.13007T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.480T>G	ENSP00000445691.1:p.Val160=
ENST00000543081.6:c.427+375T>G	ENSP00000439103.2:n.427+375T>G
ENST00000544516.6:c.157-503T>G	ENSP00000439538.2:n.157-503T>G
ENST00000545576.2:n.911T>G
ENST00000696246.1:c.465T>G	ENSP00000512504.1:p.Val155=
ENST00000696271.1:n.922T>G
ENST00000696272.1:c.495T>G	ENSP00000512515.1:p.Val165=
ENST00000696273.1:c.543T>G	ENSP00000512516.1:p.Val181=
ENST00000229335.11:c.510T>G MANE Select	ENSP00000229335.6:p.Val170=
ENST00000229335.10:c.510T>G	ENSP00000229335.6:p.Val170=
ENST00000537228.5:c.480T>G	ENSP00000445691.1:p.Val160=
ENST00000543081.5:c.423+375T>G
ENST00000544516.5:c.153-503T>G
ENST00000545512.1:c.506T>G
ENST00000545576.1:n.836T>G
NM_020661.2:c.510T>G , LRG_17t1:c.510T>G	NP_065712.1:p.Val170=
XM_011520772.1:c.480T>G	XP_011519074.1:p.Val160=
XM_011520773.1:c.427+375T>G	XP_011519075.1:n.427+375T>G
NM_001330343.1:c.480T>G	NP_001317272.1:p.Val160=
NM_020661.3:c.510T>G	NP_065712.1:p.Val170=
XM_011520773.2:c.427+375T>G	XP_011519075.1:n.427+375T>G
NM_020661.4:c.510T>G MANE Select	NP_065712.1:p.Val170=
NM_001330343.2:c.480T>G	NP_001317272.1:p.Val160=