Canonical Allele Identifier: CA2617496252

Gene: AICDA

Linked Data

• gnomAD v4: 12-8604387-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604392del , CM000674.2:g.8604392del	GRCh38
NC_000012.11:g.8756988del , CM000674.1:g.8756988del	GRCh37
NC_000012.10:g.8648255del	NCBI36
NG_011588.1:g.13459del , LRG_17:g.13459del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.514-51del	ENSP00000445691.1:n.514-51del
ENST00000543081.6:c.428-51del	ENSP00000439103.2:n.428-51del
ENST00000544516.6:c.157-51del	ENSP00000439538.2:n.157-51del
ENST00000545576.2:n.945-51del
ENST00000696246.1:c.499-51del	ENSP00000512504.1:n.499-51del
ENST00000696271.1:n.956-51del
ENST00000696272.1:c.529-51del	ENSP00000512515.1:n.529-51del
ENST00000696273.1:c.577-51del	ENSP00000512516.1:n.577-51del
ENST00000229335.11:c.544-51del MANE Select	ENSP00000229335.6:n.544-51del
ENST00000229335.10:c.544-51del	ENSP00000229335.6:n.544-51del
ENST00000537228.5:c.514-51del	ENSP00000445691.1:n.514-51del
ENST00000543081.5:c.424-51del
ENST00000544516.5:c.153-51del
ENST00000545512.1:c.540-51del
ENST00000545576.1:n.870-51del
NM_020661.2:c.544-51del , LRG_17t1:c.544-51del	NP_065712.1:n.544-51del
XM_011520772.1:c.514-51del	XP_011519074.1:n.514-51del
XM_011520773.1:c.428-51del	XP_011519075.1:n.428-51del
NM_001330343.1:c.514-51del	NP_001317272.1:n.514-51del
NM_020661.3:c.544-51del	NP_065712.1:n.544-51del
XM_011520773.2:c.428-51del	XP_011519075.1:n.428-51del
NM_020661.4:c.544-51del MANE Select	NP_065712.1:n.544-51del
NM_001330343.2:c.514-51del	NP_001317272.1:n.514-51del