Canonical Allele Identifier: CA232647025

Gene: AICDA

Linked Data

• dbSNP Id: rs374498877
• gnomAD v2: 12-8757092-TAAAA-T
• gnomAD v3: 12-8604496-TAAAA-T
• gnomAD v4: 12-8604496-TAAAA-T
• MyVariant Identifiers: chr12:g.8757095_8757098del (hg19) ; chr12:g.8757093_8757096del (hg19) ; chr12:g.8604499_8604502del (hg38) ; chr12:g.8604497_8604500del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604520_8604523del , CM000674.2:g.8604520_8604523del	GRCh38
NC_000012.11:g.8757116_8757119del , CM000674.1:g.8757116_8757119del	GRCh37
NC_000012.10:g.8648383_8648386del	NCBI36
NG_011588.1:g.13347_13350del , LRG_17:g.13347_13350del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.514-163_514-160del	ENSP00000445691.1:n.514-163_514-160del
ENST00000543081.6:c.428-163_428-160del	ENSP00000439103.2:n.428-163_428-160del
ENST00000544516.6:c.157-163_157-160del	ENSP00000439538.2:n.157-163_157-160del
ENST00000545576.2:n.945-163_945-160del
ENST00000696246.1:c.499-163_499-160del	ENSP00000512504.1:n.499-163_499-160del
ENST00000696271.1:n.956-163_956-160del
ENST00000696272.1:c.529-163_529-160del	ENSP00000512515.1:n.529-163_529-160del
ENST00000696273.1:c.577-163_577-160del	ENSP00000512516.1:n.577-163_577-160del
ENST00000229335.11:c.544-163_544-160del MANE Select	ENSP00000229335.6:n.544-163_544-160del
ENST00000229335.10:c.544-163_544-160del	ENSP00000229335.6:n.544-163_544-160del
ENST00000537228.5:c.514-163_514-160del	ENSP00000445691.1:n.514-163_514-160del
ENST00000543081.5:c.424-163_424-160del
ENST00000544516.5:c.153-163_153-160del
ENST00000545512.1:c.540-163_540-160del
ENST00000545576.1:n.870-163_870-160del
NM_020661.2:c.544-163_544-160del , LRG_17t1:c.544-163_544-160del	NP_065712.1:n.544-163_544-160del
XM_011520772.1:c.514-163_514-160del	XP_011519074.1:n.514-163_514-160del
XM_011520773.1:c.428-163_428-160del	XP_011519075.1:n.428-163_428-160del
NM_001330343.1:c.514-163_514-160del	NP_001317272.1:n.514-163_514-160del
NM_020661.3:c.544-163_544-160del	NP_065712.1:n.544-163_544-160del
XM_011520773.2:c.428-163_428-160del	XP_011519075.1:n.428-163_428-160del
NM_020661.4:c.544-163_544-160del MANE Select	NP_065712.1:n.544-163_544-160del
NM_001330343.2:c.514-163_514-160del	NP_001317272.1:n.514-163_514-160del