Canonical Allele Identifier: CA2617496271
Gene: AICDA HGNC NCBI

Linked Data

gnomAD v4: 12-8604424-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604424T>A , CM000674.2:g.8604424T>A GRCh38
NC_000012.11:g.8757020T>A , CM000674.1:g.8757020T>A GRCh37
NC_000012.10:g.8648287T>A NCBI36
NG_011588.1:g.13423A>T , LRG_17:g.13423A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000537228.6:c.514-87A>T ENSP00000445691.1:n.514-87A>T
ENST00000543081.6:c.428-87A>T ENSP00000439103.2:n.428-87A>T
ENST00000544516.6:c.157-87A>T ENSP00000439538.2:n.157-87A>T
ENST00000545576.2:n.945-87A>T
ENST00000696246.1:c.499-87A>T ENSP00000512504.1:n.499-87A>T
ENST00000696271.1:n.956-87A>T
ENST00000696272.1:c.529-87A>T ENSP00000512515.1:n.529-87A>T
ENST00000696273.1:c.577-87A>T ENSP00000512516.1:n.577-87A>T
ENST00000229335.11:c.544-87A>T MANE Select ENSP00000229335.6:n.544-87A>T
ENST00000229335.10:c.544-87A>T ENSP00000229335.6:n.544-87A>T
ENST00000537228.5:c.514-87A>T ENSP00000445691.1:n.514-87A>T
ENST00000543081.5:c.424-87A>T
ENST00000544516.5:c.153-87A>T
ENST00000545512.1:c.540-87A>T
ENST00000545576.1:n.870-87A>T
NM_020661.2:c.544-87A>T , LRG_17t1:c.544-87A>T NP_065712.1:n.544-87A>T
XM_011520772.1:c.514-87A>T XP_011519074.1:n.514-87A>T
XM_011520773.1:c.428-87A>T XP_011519075.1:n.428-87A>T
NM_001330343.1:c.514-87A>T NP_001317272.1:n.514-87A>T
NM_020661.3:c.544-87A>T NP_065712.1:n.544-87A>T
XM_011520773.2:c.428-87A>T XP_011519075.1:n.428-87A>T
NM_020661.4:c.544-87A>T MANE Select NP_065712.1:n.544-87A>T
NM_001330343.2:c.514-87A>T NP_001317272.1:n.514-87A>T