Canonical Allele Identifier: CA383817629

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757452A>T (hg19) ; chr12:g.8604856A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604856A>T , CM000674.2:g.8604856A>T	GRCh38
NC_000012.11:g.8757452A>T , CM000674.1:g.8757452A>T	GRCh37
NC_000012.10:g.8648719A>T	NCBI36
NG_011588.1:g.12991T>A , LRG_17:g.12991T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.464T>A	ENSP00000445691.1:p.Leu155Gln
ENST00000543081.6:c.427+359T>A	ENSP00000439103.2:n.427+359T>A
ENST00000544516.6:c.157-519T>A	ENSP00000439538.2:n.157-519T>A
ENST00000545576.2:n.895T>A
ENST00000696246.1:c.449T>A	ENSP00000512504.1:p.Leu150Gln
ENST00000696271.1:n.906T>A
ENST00000696272.1:c.479T>A	ENSP00000512515.1:p.Leu160Gln
ENST00000696273.1:c.527T>A	ENSP00000512516.1:p.Leu176Gln
ENST00000229335.11:c.494T>A MANE Select	ENSP00000229335.6:p.Leu165Gln
ENST00000229335.10:c.494T>A	ENSP00000229335.6:p.Leu165Gln
ENST00000537228.5:c.464T>A	ENSP00000445691.1:p.Leu155Gln
ENST00000543081.5:c.423+359T>A
ENST00000544516.5:c.153-519T>A
ENST00000545512.1:c.490T>A
ENST00000545576.1:n.820T>A
NM_020661.2:c.494T>A , LRG_17t1:c.494T>A	NP_065712.1:p.Leu165Gln
XM_011520772.1:c.464T>A	XP_011519074.1:p.Leu155Gln
XM_011520773.1:c.427+359T>A	XP_011519075.1:n.427+359T>A
NM_001330343.1:c.464T>A	NP_001317272.1:p.Leu155Gln
NM_020661.3:c.494T>A	NP_065712.1:p.Leu165Gln
XM_011520773.2:c.427+359T>A	XP_011519075.1:n.427+359T>A
NM_020661.4:c.494T>A MANE Select	NP_065712.1:p.Leu165Gln
NM_001330343.2:c.464T>A	NP_001317272.1:p.Leu155Gln