Canonical Allele Identifier: CA384038144

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8759528C>G (hg19) ; chr12:g.8606932C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8606932C>G , CM000674.2:g.8606932C>G	GRCh38
NC_000012.11:g.8759528C>G , CM000674.1:g.8759528C>G	GRCh37
NC_000012.10:g.8650795C>G	NCBI36
NG_011588.1:g.10915G>C , LRG_17:g.10915G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.89G>C	ENSP00000445691.1:p.Cys30Ser
ENST00000543081.6:c.89G>C	ENSP00000439103.2:p.Cys30Ser
ENST00000544516.6:c.89G>C	ENSP00000439538.2:p.Cys30Ser
ENST00000545576.2:n.198G>C
ENST00000696246.1:c.74G>C	ENSP00000512504.1:p.Cys25Ser
ENST00000696271.1:n.209G>C
ENST00000696272.1:c.74G>C	ENSP00000512515.1:p.Cys25Ser
ENST00000696273.1:c.122G>C	ENSP00000512516.1:p.Cys41Ser
ENST00000229335.11:c.89G>C MANE Select	ENSP00000229335.6:p.Cys30Ser
ENST00000229335.10:c.89G>C	ENSP00000229335.6:p.Cys30Ser
ENST00000537228.5:c.89G>C	ENSP00000445691.1:p.Cys30Ser
ENST00000543081.5:c.85G>C
ENST00000544516.5:c.85G>C
ENST00000545512.1:c.85G>C
ENST00000545576.1:n.123G>C
NM_020661.2:c.89G>C , LRG_17t1:c.89G>C	NP_065712.1:p.Cys30Ser
XM_011520772.1:c.89G>C	XP_011519074.1:p.Cys30Ser
XM_011520773.1:c.89G>C	XP_011519075.1:p.Cys30Ser
NM_001330343.1:c.89G>C	NP_001317272.1:p.Cys30Ser
NM_020661.3:c.89G>C	NP_065712.1:p.Cys30Ser
XM_011520773.2:c.89G>C	XP_011519075.1:p.Cys30Ser
NM_020661.4:c.89G>C MANE Select	NP_065712.1:p.Cys30Ser
NM_001330343.2:c.89G>C	NP_001317272.1:p.Cys30Ser