Canonical Allele Identifier: CA213484
Gene: AICDA HGNC NCBI

Linked Data

ClinVar Variation Id: 35655
dbSNP Id: rs193922703
gnomAD v2: 12-8757987-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8605391C>T , CM000674.2:g.8605391C>T GRCh38
NC_000012.11:g.8757987C>T , CM000674.1:g.8757987C>T GRCh37
NC_000012.10:g.8649254C>T NCBI36
NG_011588.1:g.12456G>A , LRG_17:g.12456G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000537228.6:c.251G>A ENSP00000445691.1:p.Trp84Ter
ENST00000543081.6:c.251G>A ENSP00000439103.2:p.Trp84Ter
ENST00000544516.6:c.157-1054G>A ENSP00000439538.2:n.157-1054G>A
ENST00000545576.2:n.360G>A
ENST00000696246.1:c.236G>A ENSP00000512504.1:p.Trp79Ter
ENST00000696271.1:n.371G>A
ENST00000696272.1:c.236G>A ENSP00000512515.1:p.Trp79Ter
ENST00000696273.1:c.284G>A ENSP00000512516.1:p.Trp95Ter
ENST00000229335.11:c.251G>A MANE Select ENSP00000229335.6:p.Trp84Ter
ENST00000229335.10:c.251G>A ENSP00000229335.6:p.Trp84Ter
ENST00000537228.5:c.251G>A ENSP00000445691.1:p.Trp84Ter
ENST00000543081.5:c.247G>A
ENST00000544516.5:c.153-1054G>A
ENST00000545512.1:c.247G>A
ENST00000545576.1:n.285G>A
NM_020661.2:c.251G>A , LRG_17t1:c.251G>A NP_065712.1:p.Trp84Ter
XM_011520772.1:c.251G>A XP_011519074.1:p.Trp84Ter
XM_011520773.1:c.251G>A XP_011519075.1:p.Trp84Ter
NM_001330343.1:c.251G>A NP_001317272.1:p.Trp84Ter
NM_020661.3:c.251G>A NP_065712.1:p.Trp84Ter
XM_011520773.2:c.251G>A XP_011519075.1:p.Trp84Ter
NM_020661.4:c.251G>A MANE Select NP_065712.1:p.Trp84Ter
NM_001330343.2:c.251G>A NP_001317272.1:p.Trp84Ter