Canonical Allele Identifier: CA383817979

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757504A>G (hg19) ; chr12:g.8604908A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604908A>G , CM000674.2:g.8604908A>G	GRCh38
NC_000012.11:g.8757504A>G , CM000674.1:g.8757504A>G	GRCh37
NC_000012.10:g.8648771A>G	NCBI36
NG_011588.1:g.12939T>C , LRG_17:g.12939T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.428-16T>C	ENSP00000445691.1:n.428-16T>C
ENST00000543081.6:c.427+307T>C	ENSP00000439103.2:n.427+307T>C
ENST00000544516.6:c.157-571T>C	ENSP00000439538.2:n.157-571T>C
ENST00000545576.2:n.843T>C
ENST00000696246.1:c.413-16T>C	ENSP00000512504.1:n.413-16T>C
ENST00000696271.1:n.854T>C
ENST00000696272.1:c.427T>C	ENSP00000512515.1:p.Trp143Arg
ENST00000696273.1:c.475T>C	ENSP00000512516.1:p.Trp159Arg
ENST00000229335.11:c.442T>C MANE Select	ENSP00000229335.6:p.Trp148Arg
ENST00000229335.10:c.442T>C	ENSP00000229335.6:p.Trp148Arg
ENST00000537228.5:c.428-16T>C	ENSP00000445691.1:n.428-16T>C
ENST00000543081.5:c.423+307T>C
ENST00000544516.5:c.153-571T>C
ENST00000545512.1:c.438T>C
ENST00000545576.1:n.768T>C
NM_020661.2:c.442T>C , LRG_17t1:c.442T>C	NP_065712.1:p.Trp148Arg
XM_011520772.1:c.428-16T>C	XP_011519074.1:n.428-16T>C
XM_011520773.1:c.427+307T>C	XP_011519075.1:n.427+307T>C
NM_001330343.1:c.428-16T>C	NP_001317272.1:n.428-16T>C
NM_020661.3:c.442T>C	NP_065712.1:p.Trp148Arg
XM_011520773.2:c.427+307T>C	XP_011519075.1:n.427+307T>C
NM_020661.4:c.442T>C MANE Select	NP_065712.1:p.Trp148Arg
NM_001330343.2:c.428-16T>C	NP_001317272.1:n.428-16T>C