Canonical Allele Identifier: CA383818966

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757943G>C (hg19) ; chr12:g.8605347G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8605347G>C , CM000674.2:g.8605347G>C	GRCh38
NC_000012.11:g.8757943G>C , CM000674.1:g.8757943G>C	GRCh37
NC_000012.10:g.8649210G>C	NCBI36
NG_011588.1:g.12500C>G , LRG_17:g.12500C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.295C>G	ENSP00000445691.1:p.Arg99Gly
ENST00000543081.6:c.295C>G	ENSP00000439103.2:p.Arg99Gly
ENST00000544516.6:c.157-1010C>G	ENSP00000439538.2:n.157-1010C>G
ENST00000545576.2:n.404C>G
ENST00000696246.1:c.280C>G	ENSP00000512504.1:p.Arg94Gly
ENST00000696271.1:n.415C>G
ENST00000696272.1:c.280C>G	ENSP00000512515.1:p.Arg94Gly
ENST00000696273.1:c.328C>G	ENSP00000512516.1:p.Arg110Gly
ENST00000229335.11:c.295C>G MANE Select	ENSP00000229335.6:p.Arg99Gly
ENST00000229335.10:c.295C>G	ENSP00000229335.6:p.Arg99Gly
ENST00000537228.5:c.295C>G	ENSP00000445691.1:p.Arg99Gly
ENST00000543081.5:c.291C>G
ENST00000544516.5:c.153-1010C>G
ENST00000545512.1:c.291C>G
ENST00000545576.1:n.329C>G
NM_020661.2:c.295C>G , LRG_17t1:c.295C>G	NP_065712.1:p.Arg99Gly
XM_011520772.1:c.295C>G	XP_011519074.1:p.Arg99Gly
XM_011520773.1:c.295C>G	XP_011519075.1:p.Arg99Gly
NM_001330343.1:c.295C>G	NP_001317272.1:p.Arg99Gly
NM_020661.3:c.295C>G	NP_065712.1:p.Arg99Gly
XM_011520773.2:c.295C>G	XP_011519075.1:p.Arg99Gly
NM_020661.4:c.295C>G MANE Select	NP_065712.1:p.Arg99Gly
NM_001330343.2:c.295C>G	NP_001317272.1:p.Arg99Gly