Canonical Allele Identifier: CA478291651

Gene: AICDA

Linked Data

• dbSNP Id: rs2136431076
• MyVariant Identifiers: chr12:g.8757475T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604879T>C , CM000674.2:g.8604879T>C	GRCh38
NC_000012.11:g.8757475T>C , CM000674.1:g.8757475T>C	GRCh37
NC_000012.10:g.8648742T>C	NCBI36
NG_011588.1:g.12968A>G , LRG_17:g.12968A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.441A>G	ENSP00000445691.1:p.Arg147=
ENST00000543081.6:c.427+336A>G	ENSP00000439103.2:n.427+336A>G
ENST00000544516.6:c.157-542A>G	ENSP00000439538.2:n.157-542A>G
ENST00000545576.2:n.872A>G
ENST00000696246.1:c.426A>G	ENSP00000512504.1:p.Arg142=
ENST00000696271.1:n.883A>G
ENST00000696272.1:c.456A>G	ENSP00000512515.1:p.Arg152=
ENST00000696273.1:c.504A>G	ENSP00000512516.1:p.Arg168=
ENST00000229335.11:c.471A>G MANE Select	ENSP00000229335.6:p.Arg157=
ENST00000229335.10:c.471A>G	ENSP00000229335.6:p.Arg157=
ENST00000537228.5:c.441A>G	ENSP00000445691.1:p.Arg147=
ENST00000543081.5:c.423+336A>G
ENST00000544516.5:c.153-542A>G
ENST00000545512.1:c.467A>G
ENST00000545576.1:n.797A>G
NM_020661.2:c.471A>G , LRG_17t1:c.471A>G	NP_065712.1:p.Arg157=
XM_011520772.1:c.441A>G	XP_011519074.1:p.Arg147=
XM_011520773.1:c.427+336A>G	XP_011519075.1:n.427+336A>G
NM_001330343.1:c.441A>G	NP_001317272.1:p.Arg147=
NM_020661.3:c.471A>G	NP_065712.1:p.Arg157=
XM_011520773.2:c.427+336A>G	XP_011519075.1:n.427+336A>G
NM_020661.4:c.471A>G MANE Select	NP_065712.1:p.Arg157=
NM_001330343.2:c.441A>G	NP_001317272.1:p.Arg147=