Canonical Allele Identifier: CA603490287

Gene: AICDA

Linked Data

• dbSNP Id: rs1334228132
• gnomAD v2: 12-8757837-A-AT
• gnomAD v4: 12-8605241-A-AT
• MyVariant Identifiers: chr12:g.8757837_8757838insT (hg19) ; chr12:g.8605241_8605242insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8605241_8605242insT , CM000674.2:g.8605241_8605242insT	GRCh38
NC_000012.11:g.8757837_8757838insT , CM000674.1:g.8757837_8757838insT	GRCh37
NC_000012.10:g.8649104_8649105insT	NCBI36
NG_011588.1:g.12605_12606insA , LRG_17:g.12605_12606insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.400_401insA	ENSP00000445691.1:p.Val134AspfsTer24
ENST00000543081.6:c.400_401insA	ENSP00000439103.2:p.Val134AspfsTer?
ENST00000544516.6:c.157-905_157-904insA	ENSP00000439538.2:n.157-905_157-904insA
ENST00000545576.2:n.509_510insA
ENST00000696246.1:c.385_386insA	ENSP00000512504.1:p.Val129AspfsTer24
ENST00000696271.1:n.520_521insA
ENST00000696272.1:c.385_386insA	ENSP00000512515.1:p.Val129AspfsTer?
ENST00000696273.1:c.433_434insA	ENSP00000512516.1:p.Val145AspfsTer?
ENST00000229335.11:c.400_401insA MANE Select	ENSP00000229335.6:p.Val134AspfsTer?
ENST00000229335.10:c.400_401insA	ENSP00000229335.6:p.Val134AspfsTer?
ENST00000537228.5:c.400_401insA	ENSP00000445691.1:p.Val134AspfsTer24
ENST00000543081.5:c.396_397insA
ENST00000544516.5:c.153-905_153-904insA
ENST00000545512.1:c.396_397insA
ENST00000545576.1:n.434_435insA
NM_020661.2:c.400_401insA , LRG_17t1:c.400_401insA	NP_065712.1:p.Val134AspfsTer?
XM_011520772.1:c.400_401insA	XP_011519074.1:p.Val134AspfsTer24
XM_011520773.1:c.400_401insA	XP_011519075.1:p.Val134AspfsTer?
NM_001330343.1:c.400_401insA	NP_001317272.1:p.Val134AspfsTer24
NM_020661.3:c.400_401insA	NP_065712.1:p.Val134AspfsTer?
XM_011520773.2:c.400_401insA	XP_011519075.1:p.Val134AspfsTer?
NM_020661.4:c.400_401insA MANE Select	NP_065712.1:p.Val134AspfsTer?
NM_001330343.2:c.400_401insA	NP_001317272.1:p.Val134AspfsTer24