Canonical Allele Identifier: CA2617496434

Gene: AICDA

Linked Data

• gnomAD v4: 12-8604933-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604933_8604934insG , CM000674.2:g.8604933_8604934insG	GRCh38
NC_000012.11:g.8757529_8757530insG , CM000674.1:g.8757529_8757530insG	GRCh37
NC_000012.10:g.8648796_8648797insG	NCBI36
NG_011588.1:g.12913_12914insC , LRG_17:g.12913_12914insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.428-42_428-41insC	ENSP00000445691.1:n.428-42_428-41insC
ENST00000543081.6:c.427+281_427+282insC	ENSP00000439103.2:n.427+281_427+282insC
ENST00000544516.6:c.157-597_157-596insC	ENSP00000439538.2:n.157-597_157-596insC
ENST00000545576.2:n.817_818insC
ENST00000696246.1:c.413-42_413-41insC	ENSP00000512504.1:n.413-42_413-41insC
ENST00000696271.1:n.828_829insC
ENST00000696272.1:c.413-12_413-11insC	ENSP00000512515.1:n.413-12_413-11insC
ENST00000696273.1:c.461-12_461-11insC	ENSP00000512516.1:n.461-12_461-11insC
ENST00000229335.11:c.428-12_428-11insC MANE Select	ENSP00000229335.6:n.428-12_428-11insC
ENST00000229335.10:c.428-12_428-11insC	ENSP00000229335.6:n.428-12_428-11insC
ENST00000537228.5:c.428-42_428-41insC	ENSP00000445691.1:n.428-42_428-41insC
ENST00000543081.5:c.423+281_423+282insC
ENST00000544516.5:c.153-597_153-596insC
ENST00000545512.1:c.424-12_424-11insC
ENST00000545576.1:n.742_743insC
NM_020661.2:c.428-12_428-11insC , LRG_17t1:c.428-12_428-11insC	NP_065712.1:n.428-12_428-11insC
XM_011520772.1:c.428-42_428-41insC	XP_011519074.1:n.428-42_428-41insC
XM_011520773.1:c.427+281_427+282insC	XP_011519075.1:n.427+281_427+282insC
NM_001330343.1:c.428-42_428-41insC	NP_001317272.1:n.428-42_428-41insC
NM_020661.3:c.428-12_428-11insC	NP_065712.1:n.428-12_428-11insC
XM_011520773.2:c.427+281_427+282insC	XP_011519075.1:n.427+281_427+282insC
NM_020661.4:c.428-12_428-11insC MANE Select	NP_065712.1:n.428-12_428-11insC
NM_001330343.2:c.428-42_428-41insC	NP_001317272.1:n.428-42_428-41insC