Canonical Allele Identifier: CA16043732
Gene: AICDA HGNC NCBI

Linked Data

ClinVar Variation Id: 374429
ClinVar RCV Id: RCV000415972
dbSNP Id: rs1057519097

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8606929T>C , CM000674.2:g.8606929T>C GRCh38
NC_000012.11:g.8759525T>C , CM000674.1:g.8759525T>C GRCh37
NC_000012.10:g.8650792T>C NCBI36
NG_011588.1:g.10918A>G , LRG_17:g.10918A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000537228.6:c.92A>G ENSP00000445691.1:p.Tyr31Cys
ENST00000543081.6:c.92A>G ENSP00000439103.2:p.Tyr31Cys
ENST00000544516.6:c.92A>G ENSP00000439538.2:p.Tyr31Cys
ENST00000545576.2:n.201A>G
ENST00000696246.1:c.77A>G ENSP00000512504.1:p.Tyr26Cys
ENST00000696271.1:n.212A>G
ENST00000696272.1:c.77A>G ENSP00000512515.1:p.Tyr26Cys
ENST00000696273.1:c.125A>G ENSP00000512516.1:p.Tyr42Cys
ENST00000229335.11:c.92A>G MANE Select ENSP00000229335.6:p.Tyr31Cys
ENST00000229335.10:c.92A>G ENSP00000229335.6:p.Tyr31Cys
ENST00000537228.5:c.92A>G ENSP00000445691.1:p.Tyr31Cys
ENST00000543081.5:c.88A>G
ENST00000544516.5:c.88A>G
ENST00000545512.1:c.88A>G
ENST00000545576.1:n.126A>G
NM_020661.2:c.92A>G , LRG_17t1:c.92A>G NP_065712.1:p.Tyr31Cys
XM_011520772.1:c.92A>G XP_011519074.1:p.Tyr31Cys
XM_011520773.1:c.92A>G XP_011519075.1:p.Tyr31Cys
NM_001330343.1:c.92A>G NP_001317272.1:p.Tyr31Cys
NM_020661.3:c.92A>G NP_065712.1:p.Tyr31Cys
XM_011520773.2:c.92A>G XP_011519075.1:p.Tyr31Cys
NM_020661.4:c.92A>G MANE Select NP_065712.1:p.Tyr31Cys
NM_001330343.2:c.92A>G NP_001317272.1:p.Tyr31Cys