Canonical Allele Identifier: CA6434505

Gene: AICDA

Linked Data

• dbSNP Id: rs763449075
• ExAC: 12:8759499 T / A
• gnomAD v2: 12-8759499-T-A
• MyVariant Identifiers: chr12:g.8759499T>A (hg19) ; chr12:g.8606903T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8606903T>A , CM000674.2:g.8606903T>A	GRCh38
NC_000012.11:g.8759499T>A , CM000674.1:g.8759499T>A	GRCh37
NC_000012.10:g.8650766T>A	NCBI36
NG_011588.1:g.10944A>T , LRG_17:g.10944A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.118A>T	ENSP00000445691.1:p.Thr40Ser
ENST00000543081.6:c.118A>T	ENSP00000439103.2:p.Thr40Ser
ENST00000544516.6:c.118A>T	ENSP00000439538.2:p.Thr40Ser
ENST00000545576.2:n.227A>T
ENST00000696246.1:c.103A>T	ENSP00000512504.1:p.Thr35Ser
ENST00000696271.1:n.238A>T
ENST00000696272.1:c.103A>T	ENSP00000512515.1:p.Thr35Ser
ENST00000696273.1:c.151A>T	ENSP00000512516.1:p.Thr51Ser
ENST00000229335.11:c.118A>T MANE Select	ENSP00000229335.6:p.Thr40Ser
ENST00000229335.10:c.118A>T	ENSP00000229335.6:p.Thr40Ser
ENST00000537228.5:c.118A>T	ENSP00000445691.1:p.Thr40Ser
ENST00000543081.5:c.114A>T
ENST00000544516.5:c.114A>T
ENST00000545512.1:c.114A>T
ENST00000545576.1:n.152A>T
NM_020661.2:c.118A>T , LRG_17t1:c.118A>T	NP_065712.1:p.Thr40Ser
XM_011520772.1:c.118A>T	XP_011519074.1:p.Thr40Ser
XM_011520773.1:c.118A>T	XP_011519075.1:p.Thr40Ser
NM_001330343.1:c.118A>T	NP_001317272.1:p.Thr40Ser
NM_020661.3:c.118A>T	NP_065712.1:p.Thr40Ser
XM_011520773.2:c.118A>T	XP_011519075.1:p.Thr40Ser
NM_020661.4:c.118A>T MANE Select	NP_065712.1:p.Thr40Ser
NM_001330343.2:c.118A>T	NP_001317272.1:p.Thr40Ser