Canonical Allele Identifier: CA2794483218

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604914_8604918dup , CM000674.2:g.8604914_8604918dup	GRCh38
NC_000012.11:g.8757510_8757514dup , CM000674.1:g.8757510_8757514dup	GRCh37
NC_000012.10:g.8648777_8648781dup	NCBI36
NG_011588.1:g.12929_12933dup , LRG_17:g.12929_12933dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.428-26_428-22dup	ENSP00000445691.1:n.428-26_428-22dup
ENST00000543081.6:c.427+297_427+301dup	ENSP00000439103.2:n.427+297_427+301dup
ENST00000544516.6:c.157-581_157-577dup	ENSP00000439538.2:n.157-581_157-577dup
ENST00000545576.2:n.833_837dup
ENST00000696246.1:c.413-26_413-22dup	ENSP00000512504.1:n.413-26_413-22dup
ENST00000696271.1:n.844_848dup
ENST00000696272.1:c.417_421dup	ENSP00000512515.1:p.Tyr141PhefsTer9
ENST00000696273.1:c.465_469dup	ENSP00000512516.1:p.Tyr157PhefsTer9
ENST00000229335.11:c.432_436dup MANE Select	ENSP00000229335.6:p.Tyr146PhefsTer9
ENST00000229335.10:c.432_436dup	ENSP00000229335.6:p.Tyr146PhefsTer9
ENST00000537228.5:c.428-26_428-22dup	ENSP00000445691.1:n.428-26_428-22dup
ENST00000543081.5:c.423+297_423+301dup
ENST00000544516.5:c.153-581_153-577dup
ENST00000545512.1:c.428_432dup
ENST00000545576.1:n.758_762dup
NM_020661.2:c.432_436dup , LRG_17t1:c.432_436dup	NP_065712.1:p.Tyr146PhefsTer9
XM_011520772.1:c.428-26_428-22dup	XP_011519074.1:n.428-26_428-22dup
XM_011520773.1:c.427+297_427+301dup	XP_011519075.1:n.427+297_427+301dup
NM_001330343.1:c.428-26_428-22dup	NP_001317272.1:n.428-26_428-22dup
NM_020661.3:c.432_436dup	NP_065712.1:p.Tyr146PhefsTer9
XM_011520773.2:c.427+297_427+301dup	XP_011519075.1:n.427+297_427+301dup
NM_020661.4:c.432_436dup MANE Select	NP_065712.1:p.Tyr146PhefsTer9
NM_001330343.2:c.428-26_428-22dup	NP_001317272.1:n.428-26_428-22dup