Canonical Allele Identifier: CA383817784

Gene: AICDA

Linked Data

• gnomAD v4: 12-8604878-T-C
• MyVariant Identifiers: chr12:g.8757474T>C (hg19) ; chr12:g.8604878T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604878T>C , CM000674.2:g.8604878T>C	GRCh38
NC_000012.11:g.8757474T>C , CM000674.1:g.8757474T>C	GRCh37
NC_000012.10:g.8648741T>C	NCBI36
NG_011588.1:g.12969A>G , LRG_17:g.12969A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.442A>G	ENSP00000445691.1:p.Thr148Ala
ENST00000543081.6:c.427+337A>G	ENSP00000439103.2:n.427+337A>G
ENST00000544516.6:c.157-541A>G	ENSP00000439538.2:n.157-541A>G
ENST00000545576.2:n.873A>G
ENST00000696246.1:c.427A>G	ENSP00000512504.1:p.Thr143Ala
ENST00000696271.1:n.884A>G
ENST00000696272.1:c.457A>G	ENSP00000512515.1:p.Thr153Ala
ENST00000696273.1:c.505A>G	ENSP00000512516.1:p.Thr169Ala
ENST00000229335.11:c.472A>G MANE Select	ENSP00000229335.6:p.Thr158Ala
ENST00000229335.10:c.472A>G	ENSP00000229335.6:p.Thr158Ala
ENST00000537228.5:c.442A>G	ENSP00000445691.1:p.Thr148Ala
ENST00000543081.5:c.423+337A>G
ENST00000544516.5:c.153-541A>G
ENST00000545512.1:c.468A>G
ENST00000545576.1:n.798A>G
NM_020661.2:c.472A>G , LRG_17t1:c.472A>G	NP_065712.1:p.Thr158Ala
XM_011520772.1:c.442A>G	XP_011519074.1:p.Thr148Ala
XM_011520773.1:c.427+337A>G	XP_011519075.1:n.427+337A>G
NM_001330343.1:c.442A>G	NP_001317272.1:p.Thr148Ala
NM_020661.3:c.472A>G	NP_065712.1:p.Thr158Ala
XM_011520773.2:c.427+337A>G	XP_011519075.1:n.427+337A>G
NM_020661.4:c.472A>G MANE Select	NP_065712.1:p.Thr158Ala
NM_001330343.2:c.442A>G	NP_001317272.1:p.Thr148Ala