Canonical Allele Identifier: CA478447719

Gene: AICDA

Linked Data

• dbSNP Id: rs1314298055
• gnomAD v2: 12-8759494-G-C
• COSMIC: COSM6138347
• MyVariant Identifiers: chr12:g.8759494G>C (hg19) ; chr12:g.8606898G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8606898G>C , CM000674.2:g.8606898G>C	GRCh38
NC_000012.11:g.8759494G>C , CM000674.1:g.8759494G>C	GRCh37
NC_000012.10:g.8650761G>C	NCBI36
NG_011588.1:g.10949C>G , LRG_17:g.10949C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.123C>G	ENSP00000445691.1:p.Ser41=
ENST00000543081.6:c.123C>G	ENSP00000439103.2:p.Ser41=
ENST00000544516.6:c.123C>G	ENSP00000439538.2:p.Ser41=
ENST00000545576.2:n.232C>G
ENST00000696246.1:c.108C>G	ENSP00000512504.1:p.Ser36=
ENST00000696271.1:n.243C>G
ENST00000696272.1:c.108C>G	ENSP00000512515.1:p.Ser36=
ENST00000696273.1:c.156C>G	ENSP00000512516.1:p.Ser52=
ENST00000229335.11:c.123C>G MANE Select	ENSP00000229335.6:p.Ser41=
ENST00000229335.10:c.123C>G	ENSP00000229335.6:p.Ser41=
ENST00000537228.5:c.123C>G	ENSP00000445691.1:p.Ser41=
ENST00000543081.5:c.119C>G
ENST00000544516.5:c.119C>G
ENST00000545512.1:c.119C>G
ENST00000545576.1:n.157C>G
NM_020661.2:c.123C>G , LRG_17t1:c.123C>G	NP_065712.1:p.Ser41=
XM_011520772.1:c.123C>G	XP_011519074.1:p.Ser41=
XM_011520773.1:c.123C>G	XP_011519075.1:p.Ser41=
NM_001330343.1:c.123C>G	NP_001317272.1:p.Ser41=
NM_020661.3:c.123C>G	NP_065712.1:p.Ser41=
XM_011520773.2:c.123C>G	XP_011519075.1:p.Ser41=
NM_020661.4:c.123C>G MANE Select	NP_065712.1:p.Ser41=
NM_001330343.2:c.123C>G	NP_001317272.1:p.Ser41=