Canonical Allele Identifier: CA383817415

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757416C>G (hg19) ; chr12:g.8604820C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604820C>G , CM000674.2:g.8604820C>G	GRCh38
NC_000012.11:g.8757416C>G , CM000674.1:g.8757416C>G	GRCh37
NC_000012.10:g.8648683C>G	NCBI36
NG_011588.1:g.13027G>C , LRG_17:g.13027G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.500G>C	ENSP00000445691.1:p.Arg167Pro
ENST00000543081.6:c.427+395G>C	ENSP00000439103.2:n.427+395G>C
ENST00000544516.6:c.157-483G>C	ENSP00000439538.2:n.157-483G>C
ENST00000545576.2:n.931G>C
ENST00000696246.1:c.485G>C	ENSP00000512504.1:p.Arg162Pro
ENST00000696271.1:n.942G>C
ENST00000696272.1:c.515G>C	ENSP00000512515.1:p.Arg172Pro
ENST00000696273.1:c.563G>C	ENSP00000512516.1:p.Arg188Pro
ENST00000229335.11:c.530G>C MANE Select	ENSP00000229335.6:p.Arg177Pro
ENST00000229335.10:c.530G>C	ENSP00000229335.6:p.Arg177Pro
ENST00000537228.5:c.500G>C	ENSP00000445691.1:p.Arg167Pro
ENST00000543081.5:c.423+395G>C
ENST00000544516.5:c.153-483G>C
ENST00000545512.1:c.526G>C
ENST00000545576.1:n.856G>C
NM_020661.2:c.530G>C , LRG_17t1:c.530G>C	NP_065712.1:p.Arg177Pro
XM_011520772.1:c.500G>C	XP_011519074.1:p.Arg167Pro
XM_011520773.1:c.427+395G>C	XP_011519075.1:n.427+395G>C
NM_001330343.1:c.500G>C	NP_001317272.1:p.Arg167Pro
NM_020661.3:c.530G>C	NP_065712.1:p.Arg177Pro
XM_011520773.2:c.427+395G>C	XP_011519075.1:n.427+395G>C
NM_020661.4:c.530G>C MANE Select	NP_065712.1:p.Arg177Pro
NM_001330343.2:c.500G>C	NP_001317272.1:p.Arg167Pro