Canonical Allele Identifier: CA2617496297

Gene: AICDA

Linked Data

• gnomAD v4: 12-8604452-AGTAAATTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604454_8604461del , CM000674.2:g.8604454_8604461del	GRCh38
NC_000012.11:g.8757050_8757057del , CM000674.1:g.8757050_8757057del	GRCh37
NC_000012.10:g.8648317_8648324del	NCBI36
NG_011588.1:g.13387_13394del , LRG_17:g.13387_13394del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.514-123_514-116del	ENSP00000445691.1:n.514-123_514-116del
ENST00000543081.6:c.428-123_428-116del	ENSP00000439103.2:n.428-123_428-116del
ENST00000544516.6:c.157-123_157-116del	ENSP00000439538.2:n.157-123_157-116del
ENST00000545576.2:n.945-123_945-116del
ENST00000696246.1:c.499-123_499-116del	ENSP00000512504.1:n.499-123_499-116del
ENST00000696271.1:n.956-123_956-116del
ENST00000696272.1:c.529-123_529-116del	ENSP00000512515.1:n.529-123_529-116del
ENST00000696273.1:c.577-123_577-116del	ENSP00000512516.1:n.577-123_577-116del
ENST00000229335.11:c.544-123_544-116del MANE Select	ENSP00000229335.6:n.544-123_544-116del
ENST00000229335.10:c.544-123_544-116del	ENSP00000229335.6:n.544-123_544-116del
ENST00000537228.5:c.514-123_514-116del	ENSP00000445691.1:n.514-123_514-116del
ENST00000543081.5:c.424-123_424-116del
ENST00000544516.5:c.153-123_153-116del
ENST00000545512.1:c.540-123_540-116del
ENST00000545576.1:n.870-123_870-116del
NM_020661.2:c.544-123_544-116del , LRG_17t1:c.544-123_544-116del	NP_065712.1:n.544-123_544-116del
XM_011520772.1:c.514-123_514-116del	XP_011519074.1:n.514-123_514-116del
XM_011520773.1:c.428-123_428-116del	XP_011519075.1:n.428-123_428-116del
NM_001330343.1:c.514-123_514-116del	NP_001317272.1:n.514-123_514-116del
NM_020661.3:c.544-123_544-116del	NP_065712.1:n.544-123_544-116del
XM_011520773.2:c.428-123_428-116del	XP_011519075.1:n.428-123_428-116del
NM_020661.4:c.544-123_544-116del MANE Select	NP_065712.1:n.544-123_544-116del
NM_001330343.2:c.514-123_514-116del	NP_001317272.1:n.514-123_514-116del