Canonical Allele Identifier: CA383818883

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757924C>G (hg19) ; chr12:g.8605328C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8605328C>G , CM000674.2:g.8605328C>G	GRCh38
NC_000012.11:g.8757924C>G , CM000674.1:g.8757924C>G	GRCh37
NC_000012.10:g.8649191C>G	NCBI36
NG_011588.1:g.12519G>C , LRG_17:g.12519G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.314G>C	ENSP00000445691.1:p.Ser105Thr
ENST00000543081.6:c.314G>C	ENSP00000439103.2:p.Ser105Thr
ENST00000544516.6:c.157-991G>C	ENSP00000439538.2:n.157-991G>C
ENST00000545576.2:n.423G>C
ENST00000696246.1:c.299G>C	ENSP00000512504.1:p.Ser100Thr
ENST00000696271.1:n.434G>C
ENST00000696272.1:c.299G>C	ENSP00000512515.1:p.Ser100Thr
ENST00000696273.1:c.347G>C	ENSP00000512516.1:p.Ser116Thr
ENST00000229335.11:c.314G>C MANE Select	ENSP00000229335.6:p.Ser105Thr
ENST00000229335.10:c.314G>C	ENSP00000229335.6:p.Ser105Thr
ENST00000537228.5:c.314G>C	ENSP00000445691.1:p.Ser105Thr
ENST00000543081.5:c.310G>C
ENST00000544516.5:c.153-991G>C
ENST00000545512.1:c.310G>C
ENST00000545576.1:n.348G>C
NM_020661.2:c.314G>C , LRG_17t1:c.314G>C	NP_065712.1:p.Ser105Thr
XM_011520772.1:c.314G>C	XP_011519074.1:p.Ser105Thr
XM_011520773.1:c.314G>C	XP_011519075.1:p.Ser105Thr
NM_001330343.1:c.314G>C	NP_001317272.1:p.Ser105Thr
NM_020661.3:c.314G>C	NP_065712.1:p.Ser105Thr
XM_011520773.2:c.314G>C	XP_011519075.1:p.Ser105Thr
NM_020661.4:c.314G>C MANE Select	NP_065712.1:p.Ser105Thr
NM_001330343.2:c.314G>C	NP_001317272.1:p.Ser105Thr