Canonical Allele Identifier: CA692859504

Gene: AICDA

Linked Data

• dbSNP Id: rs5796316
• gnomAD v4: 12-8604926-C-CAAAA
• MyVariant Identifiers: chr12:g.8757522_8757523insAAAA (hg19) ; chr12:g.8604926_8604927insAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604936_8604939dup , CM000674.2:g.8604936_8604939dup	GRCh38
NC_000012.11:g.8757532_8757535dup , CM000674.1:g.8757532_8757535dup	GRCh37
NC_000012.10:g.8648799_8648802dup	NCBI36
NG_011588.1:g.12917_12920dup , LRG_17:g.12917_12920dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.428-38_428-35dup	ENSP00000445691.1:n.428-38_428-35dup
ENST00000543081.6:c.427+285_427+288dup	ENSP00000439103.2:n.427+285_427+288dup
ENST00000544516.6:c.157-593_157-590dup	ENSP00000439538.2:n.157-593_157-590dup
ENST00000545576.2:n.821_824dup
ENST00000696246.1:c.413-38_413-35dup	ENSP00000512504.1:n.413-38_413-35dup
ENST00000696271.1:n.832_835dup
ENST00000696272.1:c.413-8_413-5dup	ENSP00000512515.1:n.413-8_413-5dup
ENST00000696273.1:c.461-8_461-5dup	ENSP00000512516.1:n.461-8_461-5dup
ENST00000229335.11:c.428-8_428-5dup MANE Select	ENSP00000229335.6:n.428-8_428-5dup
ENST00000229335.10:c.428-8_428-5dup	ENSP00000229335.6:n.428-8_428-5dup
ENST00000537228.5:c.428-38_428-35dup	ENSP00000445691.1:n.428-38_428-35dup
ENST00000543081.5:c.423+285_423+288dup
ENST00000544516.5:c.153-593_153-590dup
ENST00000545512.1:c.424-8_424-5dup
ENST00000545576.1:n.746_749dup
NM_020661.2:c.428-8_428-5dup , LRG_17t1:c.428-8_428-5dup	NP_065712.1:n.428-8_428-5dup
XM_011520772.1:c.428-38_428-35dup	XP_011519074.1:n.428-38_428-35dup
XM_011520773.1:c.427+285_427+288dup	XP_011519075.1:n.427+285_427+288dup
NM_001330343.1:c.428-38_428-35dup	NP_001317272.1:n.428-38_428-35dup
NM_020661.3:c.428-8_428-5dup	NP_065712.1:n.428-8_428-5dup
XM_011520773.2:c.427+285_427+288dup	XP_011519075.1:n.427+285_427+288dup
NM_020661.4:c.428-8_428-5dup MANE Select	NP_065712.1:n.428-8_428-5dup
NM_001330343.2:c.428-38_428-35dup	NP_001317272.1:n.428-38_428-35dup