Canonical Allele Identifier: CA384037991

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8759480A>G (hg19) ; chr12:g.8606884A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8606884A>G , CM000674.2:g.8606884A>G	GRCh38
NC_000012.11:g.8759480A>G , CM000674.1:g.8759480A>G	GRCh37
NC_000012.10:g.8650747A>G	NCBI36
NG_011588.1:g.10963T>C , LRG_17:g.10963T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.137T>C	ENSP00000445691.1:p.Phe46Ser
ENST00000543081.6:c.137T>C	ENSP00000439103.2:p.Phe46Ser
ENST00000544516.6:c.137T>C	ENSP00000439538.2:p.Phe46Ser
ENST00000545576.2:n.246T>C
ENST00000696246.1:c.122T>C	ENSP00000512504.1:p.Phe41Ser
ENST00000696271.1:n.257T>C
ENST00000696272.1:c.122T>C	ENSP00000512515.1:p.Phe41Ser
ENST00000696273.1:c.170T>C	ENSP00000512516.1:p.Phe57Ser
ENST00000229335.11:c.137T>C MANE Select	ENSP00000229335.6:p.Phe46Ser
ENST00000229335.10:c.137T>C	ENSP00000229335.6:p.Phe46Ser
ENST00000537228.5:c.137T>C	ENSP00000445691.1:p.Phe46Ser
ENST00000543081.5:c.133T>C
ENST00000544516.5:c.133T>C
ENST00000545512.1:c.133T>C
ENST00000545576.1:n.171T>C
NM_020661.2:c.137T>C , LRG_17t1:c.137T>C	NP_065712.1:p.Phe46Ser
XM_011520772.1:c.137T>C	XP_011519074.1:p.Phe46Ser
XM_011520773.1:c.137T>C	XP_011519075.1:p.Phe46Ser
NM_001330343.1:c.137T>C	NP_001317272.1:p.Phe46Ser
NM_020661.3:c.137T>C	NP_065712.1:p.Phe46Ser
XM_011520773.2:c.137T>C	XP_011519075.1:p.Phe46Ser
NM_020661.4:c.137T>C MANE Select	NP_065712.1:p.Phe46Ser
NM_001330343.2:c.137T>C	NP_001317272.1:p.Phe46Ser