Canonical Allele Identifier: CA384038095

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8759519A>G (hg19) ; chr12:g.8606923A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8606923A>G , CM000674.2:g.8606923A>G	GRCh38
NC_000012.11:g.8759519A>G , CM000674.1:g.8759519A>G	GRCh37
NC_000012.10:g.8650786A>G	NCBI36
NG_011588.1:g.10924T>C , LRG_17:g.10924T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.98T>C	ENSP00000445691.1:p.Val33Ala
ENST00000543081.6:c.98T>C	ENSP00000439103.2:p.Val33Ala
ENST00000544516.6:c.98T>C	ENSP00000439538.2:p.Val33Ala
ENST00000545576.2:n.207T>C
ENST00000696246.1:c.83T>C	ENSP00000512504.1:p.Val28Ala
ENST00000696271.1:n.218T>C
ENST00000696272.1:c.83T>C	ENSP00000512515.1:p.Val28Ala
ENST00000696273.1:c.131T>C	ENSP00000512516.1:p.Val44Ala
ENST00000229335.11:c.98T>C MANE Select	ENSP00000229335.6:p.Val33Ala
ENST00000229335.10:c.98T>C	ENSP00000229335.6:p.Val33Ala
ENST00000537228.5:c.98T>C	ENSP00000445691.1:p.Val33Ala
ENST00000543081.5:c.94T>C
ENST00000544516.5:c.94T>C
ENST00000545512.1:c.94T>C
ENST00000545576.1:n.132T>C
NM_020661.2:c.98T>C , LRG_17t1:c.98T>C	NP_065712.1:p.Val33Ala
XM_011520772.1:c.98T>C	XP_011519074.1:p.Val33Ala
XM_011520773.1:c.98T>C	XP_011519075.1:p.Val33Ala
NM_001330343.1:c.98T>C	NP_001317272.1:p.Val33Ala
NM_020661.3:c.98T>C	NP_065712.1:p.Val33Ala
XM_011520773.2:c.98T>C	XP_011519075.1:p.Val33Ala
NM_020661.4:c.98T>C MANE Select	NP_065712.1:p.Val33Ala
NM_001330343.2:c.98T>C	NP_001317272.1:p.Val33Ala