Canonical Allele Identifier: CA6434498

Gene: AICDA

Linked Data

• dbSNP Id: rs750190035
• ExAC: 12:8759448 CTT / C
• gnomAD v2: 12-8759448-CTT-C
• gnomAD v3: 12-8606852-CTT-C
• gnomAD v4: 12-8606852-CTT-C
• MyVariant Identifiers: chr12:g.8759449_8759450del (hg19) ; chr12:g.8606853_8606854del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8606854_8606855del , CM000674.2:g.8606854_8606855del	GRCh38
NC_000012.11:g.8759450_8759451del , CM000674.1:g.8759450_8759451del	GRCh37
NC_000012.10:g.8650717_8650718del	NCBI36
NG_011588.1:g.10993_10994del , LRG_17:g.10993_10994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.156+11_156+12del	ENSP00000445691.1:n.156+11_156+12del
ENST00000543081.6:c.156+11_156+12del	ENSP00000439103.2:n.156+11_156+12del
ENST00000544516.6:c.156+11_156+12del	ENSP00000439538.2:n.156+11_156+12del
ENST00000545576.2:n.265+11_265+12del
ENST00000696246.1:c.141+11_141+12del	ENSP00000512504.1:n.141+11_141+12del
ENST00000696271.1:n.276+11_276+12del
ENST00000696272.1:c.141+11_141+12del	ENSP00000512515.1:n.141+11_141+12del
ENST00000696273.1:c.189+11_189+12del	ENSP00000512516.1:n.189+11_189+12del
ENST00000229335.11:c.156+11_156+12del MANE Select	ENSP00000229335.6:n.156+11_156+12del
ENST00000229335.10:c.156+11_156+12del	ENSP00000229335.6:n.156+11_156+12del
ENST00000537228.5:c.156+11_156+12del	ENSP00000445691.1:n.156+11_156+12del
ENST00000543081.5:c.152+11_152+12del
ENST00000544516.5:c.152+11_152+12del
ENST00000545512.1:c.152+11_152+12del
ENST00000545576.1:n.190+11_190+12del
NM_020661.2:c.156+11_156+12del , LRG_17t1:c.156+11_156+12del	NP_065712.1:n.156+11_156+12del
XM_011520772.1:c.156+11_156+12del	XP_011519074.1:n.156+11_156+12del
XM_011520773.1:c.156+11_156+12del	XP_011519075.1:n.156+11_156+12del
NM_001330343.1:c.156+11_156+12del	NP_001317272.1:n.156+11_156+12del
NM_020661.3:c.156+11_156+12del	NP_065712.1:n.156+11_156+12del
XM_011520773.2:c.156+11_156+12del	XP_011519075.1:n.156+11_156+12del
NM_020661.4:c.156+11_156+12del MANE Select	NP_065712.1:n.156+11_156+12del
NM_001330343.2:c.156+11_156+12del	NP_001317272.1:n.156+11_156+12del