Canonical Allele Identifier: CA383818989

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757951T>G (hg19) ; chr12:g.8605355T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8605355T>G , CM000674.2:g.8605355T>G	GRCh38
NC_000012.11:g.8757951T>G , CM000674.1:g.8757951T>G	GRCh37
NC_000012.10:g.8649218T>G	NCBI36
NG_011588.1:g.12492A>C , LRG_17:g.12492A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.287A>C	ENSP00000445691.1:p.Asp96Ala
ENST00000543081.6:c.287A>C	ENSP00000439103.2:p.Asp96Ala
ENST00000544516.6:c.157-1018A>C	ENSP00000439538.2:n.157-1018A>C
ENST00000545576.2:n.396A>C
ENST00000696246.1:c.272A>C	ENSP00000512504.1:p.Asp91Ala
ENST00000696271.1:n.407A>C
ENST00000696272.1:c.272A>C	ENSP00000512515.1:p.Asp91Ala
ENST00000696273.1:c.320A>C	ENSP00000512516.1:p.Asp107Ala
ENST00000229335.11:c.287A>C MANE Select	ENSP00000229335.6:p.Asp96Ala
ENST00000229335.10:c.287A>C	ENSP00000229335.6:p.Asp96Ala
ENST00000537228.5:c.287A>C	ENSP00000445691.1:p.Asp96Ala
ENST00000543081.5:c.283A>C
ENST00000544516.5:c.153-1018A>C
ENST00000545512.1:c.283A>C
ENST00000545576.1:n.321A>C
NM_020661.2:c.287A>C , LRG_17t1:c.287A>C	NP_065712.1:p.Asp96Ala
XM_011520772.1:c.287A>C	XP_011519074.1:p.Asp96Ala
XM_011520773.1:c.287A>C	XP_011519075.1:p.Asp96Ala
NM_001330343.1:c.287A>C	NP_001317272.1:p.Asp96Ala
NM_020661.3:c.287A>C	NP_065712.1:p.Asp96Ala
XM_011520773.2:c.287A>C	XP_011519075.1:p.Asp96Ala
NM_020661.4:c.287A>C MANE Select	NP_065712.1:p.Asp96Ala
NM_001330343.2:c.287A>C	NP_001317272.1:p.Asp96Ala