Canonical Allele Identifier: CA603209601

Gene: AICDA

Linked Data

• dbSNP Id: rs1392733997
• gnomAD v2: 12-8756976-A-G
• gnomAD v4: 12-8604380-A-G
• MyVariant Identifiers: chr12:g.8756976A>G (hg19) ; chr12:g.8604380A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604380A>G , CM000674.2:g.8604380A>G	GRCh38
NC_000012.11:g.8756976A>G , CM000674.1:g.8756976A>G	GRCh37
NC_000012.10:g.8648243A>G	NCBI36
NG_011588.1:g.13467T>C , LRG_17:g.13467T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.514-43T>C	ENSP00000445691.1:n.514-43T>C
ENST00000543081.6:c.428-43T>C	ENSP00000439103.2:n.428-43T>C
ENST00000544516.6:c.157-43T>C	ENSP00000439538.2:n.157-43T>C
ENST00000545576.2:n.945-43T>C
ENST00000696246.1:c.499-43T>C	ENSP00000512504.1:n.499-43T>C
ENST00000696271.1:n.956-43T>C
ENST00000696272.1:c.529-43T>C	ENSP00000512515.1:n.529-43T>C
ENST00000696273.1:c.577-43T>C	ENSP00000512516.1:n.577-43T>C
ENST00000229335.11:c.544-43T>C MANE Select	ENSP00000229335.6:n.544-43T>C
ENST00000229335.10:c.544-43T>C	ENSP00000229335.6:n.544-43T>C
ENST00000537228.5:c.514-43T>C	ENSP00000445691.1:n.514-43T>C
ENST00000543081.5:c.424-43T>C
ENST00000544516.5:c.153-43T>C
ENST00000545512.1:c.540-43T>C
ENST00000545576.1:n.870-43T>C
NM_020661.2:c.544-43T>C , LRG_17t1:c.544-43T>C	NP_065712.1:n.544-43T>C
XM_011520772.1:c.514-43T>C	XP_011519074.1:n.514-43T>C
XM_011520773.1:c.428-43T>C	XP_011519075.1:n.428-43T>C
NM_001330343.1:c.514-43T>C	NP_001317272.1:n.514-43T>C
NM_020661.3:c.544-43T>C	NP_065712.1:n.544-43T>C
XM_011520773.2:c.428-43T>C	XP_011519075.1:n.428-43T>C
NM_020661.4:c.544-43T>C MANE Select	NP_065712.1:n.544-43T>C
NM_001330343.2:c.514-43T>C	NP_001317272.1:n.514-43T>C