Canonical Allele Identifier: CA2617496317

Gene: AICDA

Linked Data

• gnomAD v4: 12-8604474-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604475_8604476dup , CM000674.2:g.8604475_8604476dup	GRCh38
NC_000012.11:g.8757071_8757072dup , CM000674.1:g.8757071_8757072dup	GRCh37
NC_000012.10:g.8648338_8648339dup	NCBI36
NG_011588.1:g.13371_13372dup , LRG_17:g.13371_13372dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.514-139_514-138dup	ENSP00000445691.1:n.514-139_514-138dup
ENST00000543081.6:c.428-139_428-138dup	ENSP00000439103.2:n.428-139_428-138dup
ENST00000544516.6:c.157-139_157-138dup	ENSP00000439538.2:n.157-139_157-138dup
ENST00000545576.2:n.945-139_945-138dup
ENST00000696246.1:c.499-139_499-138dup	ENSP00000512504.1:n.499-139_499-138dup
ENST00000696271.1:n.956-139_956-138dup
ENST00000696272.1:c.529-139_529-138dup	ENSP00000512515.1:n.529-139_529-138dup
ENST00000696273.1:c.577-139_577-138dup	ENSP00000512516.1:n.577-139_577-138dup
ENST00000229335.11:c.544-139_544-138dup MANE Select	ENSP00000229335.6:n.544-139_544-138dup
ENST00000229335.10:c.544-139_544-138dup	ENSP00000229335.6:n.544-139_544-138dup
ENST00000537228.5:c.514-139_514-138dup	ENSP00000445691.1:n.514-139_514-138dup
ENST00000543081.5:c.424-139_424-138dup
ENST00000544516.5:c.153-139_153-138dup
ENST00000545512.1:c.540-139_540-138dup
ENST00000545576.1:n.870-139_870-138dup
NM_020661.2:c.544-139_544-138dup , LRG_17t1:c.544-139_544-138dup	NP_065712.1:n.544-139_544-138dup
XM_011520772.1:c.514-139_514-138dup	XP_011519074.1:n.514-139_514-138dup
XM_011520773.1:c.428-139_428-138dup	XP_011519075.1:n.428-139_428-138dup
NM_001330343.1:c.514-139_514-138dup	NP_001317272.1:n.514-139_514-138dup
NM_020661.3:c.544-139_544-138dup	NP_065712.1:n.544-139_544-138dup
XM_011520773.2:c.428-139_428-138dup	XP_011519075.1:n.428-139_428-138dup
NM_020661.4:c.544-139_544-138dup MANE Select	NP_065712.1:n.544-139_544-138dup
NM_001330343.2:c.514-139_514-138dup	NP_001317272.1:n.514-139_514-138dup