Canonical Allele Identifier: CA383817925

Gene: AICDA

Linked Data

• dbSNP Id: rs1409664577
• gnomAD v2: 12-8757498-T-C
• gnomAD v3: 12-8604902-T-C
• gnomAD v4: 12-8604902-T-C
• MyVariant Identifiers: chr12:g.8757498T>C (hg19) ; chr12:g.8604902T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604902T>C , CM000674.2:g.8604902T>C	GRCh38
NC_000012.11:g.8757498T>C , CM000674.1:g.8757498T>C	GRCh37
NC_000012.10:g.8648765T>C	NCBI36
NG_011588.1:g.12945A>G , LRG_17:g.12945A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.428-10A>G	ENSP00000445691.1:n.428-10A>G
ENST00000543081.6:c.427+313A>G	ENSP00000439103.2:n.427+313A>G
ENST00000544516.6:c.157-565A>G	ENSP00000439538.2:n.157-565A>G
ENST00000545576.2:n.849A>G
ENST00000696246.1:c.413-10A>G	ENSP00000512504.1:n.413-10A>G
ENST00000696271.1:n.860A>G
ENST00000696272.1:c.433A>G	ENSP00000512515.1:p.Thr145Ala
ENST00000696273.1:c.481A>G	ENSP00000512516.1:p.Thr161Ala
ENST00000229335.11:c.448A>G MANE Select	ENSP00000229335.6:p.Thr150Ala
ENST00000229335.10:c.448A>G	ENSP00000229335.6:p.Thr150Ala
ENST00000537228.5:c.428-10A>G	ENSP00000445691.1:n.428-10A>G
ENST00000543081.5:c.423+313A>G
ENST00000544516.5:c.153-565A>G
ENST00000545512.1:c.444A>G
ENST00000545576.1:n.774A>G
NM_020661.2:c.448A>G , LRG_17t1:c.448A>G	NP_065712.1:p.Thr150Ala
XM_011520772.1:c.428-10A>G	XP_011519074.1:n.428-10A>G
XM_011520773.1:c.427+313A>G	XP_011519075.1:n.427+313A>G
NM_001330343.1:c.428-10A>G	NP_001317272.1:n.428-10A>G
NM_020661.3:c.448A>G	NP_065712.1:p.Thr150Ala
XM_011520773.2:c.427+313A>G	XP_011519075.1:n.427+313A>G
NM_020661.4:c.448A>G MANE Select	NP_065712.1:p.Thr150Ala
NM_001330343.2:c.428-10A>G	NP_001317272.1:n.428-10A>G