Canonical Allele Identifier: CA6434508

Gene: AICDA

Linked Data

• dbSNP Id: rs762778537
• ExAC: 12:8759508 C / CA
• gnomAD v4: 12-8606912-C-CA
• MyVariant Identifiers: chr12:g.8759508_8759509insA (hg19) ; chr12:g.8606912_8606913insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8606913dup , CM000674.2:g.8606913dup	GRCh38
NC_000012.11:g.8759509dup , CM000674.1:g.8759509dup	GRCh37
NC_000012.10:g.8650776dup	NCBI36
NG_011588.1:g.10934dup , LRG_17:g.10934dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.108dup	ENSP00000445691.1:p.Asp37Ter
ENST00000543081.6:c.108dup	ENSP00000439103.2:p.Asp37Ter
ENST00000544516.6:c.108dup	ENSP00000439538.2:p.Asp37Ter
ENST00000545576.2:n.217dup
ENST00000696246.1:c.93dup	ENSP00000512504.1:p.Asp32Ter
ENST00000696271.1:n.228dup
ENST00000696272.1:c.93dup	ENSP00000512515.1:p.Asp32Ter
ENST00000696273.1:c.141dup	ENSP00000512516.1:p.Asp48Ter
ENST00000229335.11:c.108dup MANE Select	ENSP00000229335.6:p.Asp37Ter
ENST00000229335.10:c.108dup	ENSP00000229335.6:p.Asp37Ter
ENST00000537228.5:c.108dup	ENSP00000445691.1:p.Asp37Ter
ENST00000543081.5:c.104dup
ENST00000544516.5:c.104dup
ENST00000545512.1:c.104dup
ENST00000545576.1:n.142dup
NM_020661.2:c.108dup , LRG_17t1:c.108dup	NP_065712.1:p.Asp37Ter
XM_011520772.1:c.108dup	XP_011519074.1:p.Asp37Ter
XM_011520773.1:c.108dup	XP_011519075.1:p.Asp37Ter
NM_001330343.1:c.108dup	NP_001317272.1:p.Asp37Ter
NM_020661.3:c.108dup	NP_065712.1:p.Asp37Ter
XM_011520773.2:c.108dup	XP_011519075.1:p.Asp37Ter
NM_020661.4:c.108dup MANE Select	NP_065712.1:p.Asp37Ter
NM_001330343.2:c.108dup	NP_001317272.1:p.Asp37Ter