Canonical Allele Identifier: CA603490263

Gene: AICDA

Linked Data

• dbSNP Id: rs1491439812
• gnomAD v2: 12-8757520-TTC-T
• gnomAD v3: 12-8604924-TTC-T
• gnomAD v4: 12-8604924-TTC-T
• MyVariant Identifiers: chr12:g.8757521_8757522del (hg19) ; chr12:g.8604925_8604926del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604925_8604926del , CM000674.2:g.8604925_8604926del	GRCh38
NC_000012.11:g.8757521_8757522del , CM000674.1:g.8757521_8757522del	GRCh37
NC_000012.10:g.8648788_8648789del	NCBI36
NG_011588.1:g.12921_12922del , LRG_17:g.12921_12922del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.428-34_428-33del	ENSP00000445691.1:n.428-34_428-33del
ENST00000543081.6:c.427+289_427+290del	ENSP00000439103.2:n.427+289_427+290del
ENST00000544516.6:c.157-589_157-588del	ENSP00000439538.2:n.157-589_157-588del
ENST00000545576.2:n.825_826del
ENST00000696246.1:c.413-34_413-33del	ENSP00000512504.1:n.413-34_413-33del
ENST00000696271.1:n.836_837del
ENST00000696272.1:c.413-4_413-3del	ENSP00000512515.1:n.413-4_413-3del
ENST00000696273.1:c.461-4_461-3del	ENSP00000512516.1:n.461-4_461-3del
ENST00000229335.11:c.428-4_428-3del MANE Select	ENSP00000229335.6:n.428-4_428-3del
ENST00000229335.10:c.428-4_428-3del	ENSP00000229335.6:n.428-4_428-3del
ENST00000537228.5:c.428-34_428-33del	ENSP00000445691.1:n.428-34_428-33del
ENST00000543081.5:c.423+289_423+290del
ENST00000544516.5:c.153-589_153-588del
ENST00000545512.1:c.424-4_424-3del
ENST00000545576.1:n.750_751del
NM_020661.2:c.428-4_428-3del , LRG_17t1:c.428-4_428-3del	NP_065712.1:n.428-4_428-3del
XM_011520772.1:c.428-34_428-33del	XP_011519074.1:n.428-34_428-33del
XM_011520773.1:c.427+289_427+290del	XP_011519075.1:n.427+289_427+290del
NM_001330343.1:c.428-34_428-33del	NP_001317272.1:n.428-34_428-33del
NM_020661.3:c.428-4_428-3del	NP_065712.1:n.428-4_428-3del
XM_011520773.2:c.427+289_427+290del	XP_011519075.1:n.427+289_427+290del
NM_020661.4:c.428-4_428-3del MANE Select	NP_065712.1:n.428-4_428-3del
NM_001330343.2:c.428-34_428-33del	NP_001317272.1:n.428-34_428-33del