Canonical Allele Identifier: CA478530412

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757932G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8605336G>T , CM000674.2:g.8605336G>T	GRCh38
NC_000012.11:g.8757932G>T , CM000674.1:g.8757932G>T	GRCh37
NC_000012.10:g.8649199G>T	NCBI36
NG_011588.1:g.12511C>A , LRG_17:g.12511C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.306C>A	ENSP00000445691.1:p.Pro102=
ENST00000543081.6:c.306C>A	ENSP00000439103.2:p.Pro102=
ENST00000544516.6:c.157-999C>A	ENSP00000439538.2:n.157-999C>A
ENST00000545576.2:n.415C>A
ENST00000696246.1:c.291C>A	ENSP00000512504.1:p.Pro97=
ENST00000696271.1:n.426C>A
ENST00000696272.1:c.291C>A	ENSP00000512515.1:p.Pro97=
ENST00000696273.1:c.339C>A	ENSP00000512516.1:p.Pro113=
ENST00000229335.11:c.306C>A MANE Select	ENSP00000229335.6:p.Pro102=
ENST00000229335.10:c.306C>A	ENSP00000229335.6:p.Pro102=
ENST00000537228.5:c.306C>A	ENSP00000445691.1:p.Pro102=
ENST00000543081.5:c.302C>A
ENST00000544516.5:c.153-999C>A
ENST00000545512.1:c.302C>A
ENST00000545576.1:n.340C>A
NM_020661.2:c.306C>A , LRG_17t1:c.306C>A	NP_065712.1:p.Pro102=
XM_011520772.1:c.306C>A	XP_011519074.1:p.Pro102=
XM_011520773.1:c.306C>A	XP_011519075.1:p.Pro102=
NM_001330343.1:c.306C>A	NP_001317272.1:p.Pro102=
NM_020661.3:c.306C>A	NP_065712.1:p.Pro102=
XM_011520773.2:c.306C>A	XP_011519075.1:p.Pro102=
NM_020661.4:c.306C>A MANE Select	NP_065712.1:p.Pro102=
NM_001330343.2:c.306C>A	NP_001317272.1:p.Pro102=