Canonical Allele Identifier: CA478291358

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757412G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604816G>A , CM000674.2:g.8604816G>A	GRCh38
NC_000012.11:g.8757412G>A , CM000674.1:g.8757412G>A	GRCh37
NC_000012.10:g.8648679G>A	NCBI36
NG_011588.1:g.13031C>T , LRG_17:g.13031C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.504C>T	ENSP00000445691.1:p.Arg168=
ENST00000543081.6:c.427+399C>T	ENSP00000439103.2:n.427+399C>T
ENST00000544516.6:c.157-479C>T	ENSP00000439538.2:n.157-479C>T
ENST00000545576.2:n.935C>T
ENST00000696246.1:c.489C>T	ENSP00000512504.1:p.Arg163=
ENST00000696271.1:n.946C>T
ENST00000696272.1:c.519C>T	ENSP00000512515.1:p.Arg173=
ENST00000696273.1:c.567C>T	ENSP00000512516.1:p.Arg189=
ENST00000229335.11:c.534C>T MANE Select	ENSP00000229335.6:p.Arg178=
ENST00000229335.10:c.534C>T	ENSP00000229335.6:p.Arg178=
ENST00000537228.5:c.504C>T	ENSP00000445691.1:p.Arg168=
ENST00000543081.5:c.423+399C>T
ENST00000544516.5:c.153-479C>T
ENST00000545512.1:c.530C>T
ENST00000545576.1:n.860C>T
NM_020661.2:c.534C>T , LRG_17t1:c.534C>T	NP_065712.1:p.Arg178=
XM_011520772.1:c.504C>T	XP_011519074.1:p.Arg168=
XM_011520773.1:c.427+399C>T	XP_011519075.1:n.427+399C>T
NM_001330343.1:c.504C>T	NP_001317272.1:p.Arg168=
NM_020661.3:c.534C>T	NP_065712.1:p.Arg178=
XM_011520773.2:c.427+399C>T	XP_011519075.1:n.427+399C>T
NM_020661.4:c.534C>T MANE Select	NP_065712.1:p.Arg178=
NM_001330343.2:c.504C>T	NP_001317272.1:p.Arg168=