Canonical Allele Identifier: CA383817579

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757444T>G (hg19) ; chr12:g.8604848T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604848T>G , CM000674.2:g.8604848T>G	GRCh38
NC_000012.11:g.8757444T>G , CM000674.1:g.8757444T>G	GRCh37
NC_000012.10:g.8648711T>G	NCBI36
NG_011588.1:g.12999A>C , LRG_17:g.12999A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.472A>C	ENSP00000445691.1:p.Asn158His
ENST00000543081.6:c.427+367A>C	ENSP00000439103.2:n.427+367A>C
ENST00000544516.6:c.157-511A>C	ENSP00000439538.2:n.157-511A>C
ENST00000545576.2:n.903A>C
ENST00000696246.1:c.457A>C	ENSP00000512504.1:p.Asn153His
ENST00000696271.1:n.914A>C
ENST00000696272.1:c.487A>C	ENSP00000512515.1:p.Asn163His
ENST00000696273.1:c.535A>C	ENSP00000512516.1:p.Asn179His
ENST00000229335.11:c.502A>C MANE Select	ENSP00000229335.6:p.Asn168His
ENST00000229335.10:c.502A>C	ENSP00000229335.6:p.Asn168His
ENST00000537228.5:c.472A>C	ENSP00000445691.1:p.Asn158His
ENST00000543081.5:c.423+367A>C
ENST00000544516.5:c.153-511A>C
ENST00000545512.1:c.498A>C
ENST00000545576.1:n.828A>C
NM_020661.2:c.502A>C , LRG_17t1:c.502A>C	NP_065712.1:p.Asn168His
XM_011520772.1:c.472A>C	XP_011519074.1:p.Asn158His
XM_011520773.1:c.427+367A>C	XP_011519075.1:n.427+367A>C
NM_001330343.1:c.472A>C	NP_001317272.1:p.Asn158His
NM_020661.3:c.502A>C	NP_065712.1:p.Asn168His
XM_011520773.2:c.427+367A>C	XP_011519075.1:n.427+367A>C
NM_020661.4:c.502A>C MANE Select	NP_065712.1:p.Asn168His
NM_001330343.2:c.472A>C	NP_001317272.1:p.Asn158His