Canonical Allele Identifier: CA2617496323

Gene: AICDA

Linked Data

• gnomAD v4: 12-8604485-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604488del , CM000674.2:g.8604488del	GRCh38
NC_000012.11:g.8757084del , CM000674.1:g.8757084del	GRCh37
NC_000012.10:g.8648351del	NCBI36
NG_011588.1:g.13361del , LRG_17:g.13361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.514-149del	ENSP00000445691.1:n.514-149del
ENST00000543081.6:c.428-149del	ENSP00000439103.2:n.428-149del
ENST00000544516.6:c.157-149del	ENSP00000439538.2:n.157-149del
ENST00000545576.2:n.945-149del
ENST00000696246.1:c.499-149del	ENSP00000512504.1:n.499-149del
ENST00000696271.1:n.956-149del
ENST00000696272.1:c.529-149del	ENSP00000512515.1:n.529-149del
ENST00000696273.1:c.577-149del	ENSP00000512516.1:n.577-149del
ENST00000229335.11:c.544-149del MANE Select	ENSP00000229335.6:n.544-149del
ENST00000229335.10:c.544-149del	ENSP00000229335.6:n.544-149del
ENST00000537228.5:c.514-149del	ENSP00000445691.1:n.514-149del
ENST00000543081.5:c.424-149del
ENST00000544516.5:c.153-149del
ENST00000545512.1:c.540-149del
ENST00000545576.1:n.870-149del
NM_020661.2:c.544-149del , LRG_17t1:c.544-149del	NP_065712.1:n.544-149del
XM_011520772.1:c.514-149del	XP_011519074.1:n.514-149del
XM_011520773.1:c.428-149del	XP_011519075.1:n.428-149del
NM_001330343.1:c.514-149del	NP_001317272.1:n.514-149del
NM_020661.3:c.544-149del	NP_065712.1:n.544-149del
XM_011520773.2:c.428-149del	XP_011519075.1:n.428-149del
NM_020661.4:c.544-149del MANE Select	NP_065712.1:n.544-149del
NM_001330343.2:c.514-149del	NP_001317272.1:n.514-149del