Canonical Allele Identifier: CA2741228573

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604761_8604762dup , CM000674.2:g.8604761_8604762dup	GRCh38
NC_000012.11:g.8757357_8757358dup , CM000674.1:g.8757357_8757358dup	GRCh37
NC_000012.10:g.8648624_8648625dup	NCBI36
NG_011588.1:g.13085_13086dup , LRG_17:g.13085_13086dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.513+45_513+46dup	ENSP00000445691.1:n.513+45_513+46dup
ENST00000543081.6:c.428-425_428-424dup	ENSP00000439103.2:n.428-425_428-424dup
ENST00000544516.6:c.157-425_157-424dup	ENSP00000439538.2:n.157-425_157-424dup
ENST00000545576.2:n.944+45_944+46dup
ENST00000696246.1:c.498+45_498+46dup	ENSP00000512504.1:n.498+45_498+46dup
ENST00000696271.1:n.955+45_955+46dup
ENST00000696272.1:c.528+45_528+46dup	ENSP00000512515.1:n.528+45_528+46dup
ENST00000696273.1:c.576+45_576+46dup	ENSP00000512516.1:n.576+45_576+46dup
ENST00000229335.11:c.543+45_543+46dup MANE Select	ENSP00000229335.6:n.543+45_543+46dup
ENST00000229335.10:c.543+45_543+46dup	ENSP00000229335.6:n.543+45_543+46dup
ENST00000537228.5:c.513+45_513+46dup	ENSP00000445691.1:n.513+45_513+46dup
ENST00000543081.5:c.424-425_424-424dup
ENST00000544516.5:c.153-425_153-424dup
ENST00000545512.1:c.539+45_539+46dup
ENST00000545576.1:n.869+45_869+46dup
NM_020661.2:c.543+45_543+46dup , LRG_17t1:c.543+45_543+46dup	NP_065712.1:n.543+45_543+46dup
XM_011520772.1:c.513+45_513+46dup	XP_011519074.1:n.513+45_513+46dup
XM_011520773.1:c.428-425_428-424dup	XP_011519075.1:n.428-425_428-424dup
NM_001330343.1:c.513+45_513+46dup	NP_001317272.1:n.513+45_513+46dup
NM_020661.3:c.543+45_543+46dup	NP_065712.1:n.543+45_543+46dup
XM_011520773.2:c.428-425_428-424dup	XP_011519075.1:n.428-425_428-424dup
NM_020661.4:c.543+45_543+46dup MANE Select	NP_065712.1:n.543+45_543+46dup
NM_001330343.2:c.513+45_513+46dup	NP_001317272.1:n.513+45_513+46dup