Canonical Allele Identifier: CA383817782

Gene: AICDA

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.442A>T	ENSP00000445691.1:p.Thr148Ser
ENST00000543081.6:c.427+337A>T	ENSP00000439103.2:n.427+337A>T
ENST00000544516.6:c.157-541A>T	ENSP00000439538.2:n.157-541A>T
ENST00000545576.2:n.873A>T
ENST00000696246.1:c.427A>T	ENSP00000512504.1:p.Thr143Ser
ENST00000696271.1:n.884A>T
ENST00000696272.1:c.457A>T	ENSP00000512515.1:p.Thr153Ser
ENST00000696273.1:c.505A>T	ENSP00000512516.1:p.Thr169Ser
ENST00000229335.11:c.472A>T MANE Select	ENSP00000229335.6:p.Thr158Ser
ENST00000229335.10:c.472A>T	ENSP00000229335.6:p.Thr158Ser
ENST00000537228.5:c.442A>T	ENSP00000445691.1:p.Thr148Ser
ENST00000543081.5:c.423+337A>T
ENST00000544516.5:c.153-541A>T
ENST00000545512.1:c.468A>T
ENST00000545576.1:n.798A>T
NM_020661.2:c.472A>T , LRG_17t1:c.472A>T	NP_065712.1:p.Thr158Ser
XM_011520772.1:c.442A>T	XP_011519074.1:p.Thr148Ser
XM_011520773.1:c.427+337A>T	XP_011519075.1:n.427+337A>T
NM_001330343.1:c.442A>T	NP_001317272.1:p.Thr148Ser
NM_020661.3:c.472A>T	NP_065712.1:p.Thr158Ser
XM_011520773.2:c.427+337A>T	XP_011519075.1:n.427+337A>T
NM_020661.4:c.472A>T MANE Select	NP_065712.1:p.Thr158Ser
NM_001330343.2:c.442A>T	NP_001317272.1:p.Thr148Ser