Canonical Allele Identifier: CA383817394

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757410A>G (hg19) ; chr12:g.8604814A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604814A>G , CM000674.2:g.8604814A>G	GRCh38
NC_000012.11:g.8757410A>G , CM000674.1:g.8757410A>G	GRCh37
NC_000012.10:g.8648677A>G	NCBI36
NG_011588.1:g.13033T>C , LRG_17:g.13033T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.506T>C	ENSP00000445691.1:p.Ile169Thr
ENST00000543081.6:c.427+401T>C	ENSP00000439103.2:n.427+401T>C
ENST00000544516.6:c.157-477T>C	ENSP00000439538.2:n.157-477T>C
ENST00000545576.2:n.937T>C
ENST00000696246.1:c.491T>C	ENSP00000512504.1:p.Ile164Thr
ENST00000696271.1:n.948T>C
ENST00000696272.1:c.521T>C	ENSP00000512515.1:p.Ile174Thr
ENST00000696273.1:c.569T>C	ENSP00000512516.1:p.Ile190Thr
ENST00000229335.11:c.536T>C MANE Select	ENSP00000229335.6:p.Ile179Thr
ENST00000229335.10:c.536T>C	ENSP00000229335.6:p.Ile179Thr
ENST00000537228.5:c.506T>C	ENSP00000445691.1:p.Ile169Thr
ENST00000543081.5:c.423+401T>C
ENST00000544516.5:c.153-477T>C
ENST00000545512.1:c.532T>C
ENST00000545576.1:n.862T>C
NM_020661.2:c.536T>C , LRG_17t1:c.536T>C	NP_065712.1:p.Ile179Thr
XM_011520772.1:c.506T>C	XP_011519074.1:p.Ile169Thr
XM_011520773.1:c.427+401T>C	XP_011519075.1:n.427+401T>C
NM_001330343.1:c.506T>C	NP_001317272.1:p.Ile169Thr
NM_020661.3:c.536T>C	NP_065712.1:p.Ile179Thr
XM_011520773.2:c.427+401T>C	XP_011519075.1:n.427+401T>C
NM_020661.4:c.536T>C MANE Select	NP_065712.1:p.Ile179Thr
NM_001330343.2:c.506T>C	NP_001317272.1:p.Ile169Thr