Canonical Allele Identifier: CA944538159
Gene: AICDA HGNC NCBI

Linked Data

dbSNP Id: rs1941253897
gnomAD v3: 12-8604925-T-C
gnomAD v4: 12-8604925-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604925T>C , CM000674.2:g.8604925T>C GRCh38
NC_000012.11:g.8757521T>C , CM000674.1:g.8757521T>C GRCh37
NC_000012.10:g.8648788T>C NCBI36
NG_011588.1:g.12922A>G , LRG_17:g.12922A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000537228.6:c.428-33A>G ENSP00000445691.1:n.428-33A>G
ENST00000543081.6:c.427+290A>G ENSP00000439103.2:n.427+290A>G
ENST00000544516.6:c.157-588A>G ENSP00000439538.2:n.157-588A>G
ENST00000545576.2:n.826A>G
ENST00000696246.1:c.413-33A>G ENSP00000512504.1:n.413-33A>G
ENST00000696271.1:n.837A>G
ENST00000696272.1:c.413-3A>G ENSP00000512515.1:n.413-3A>G
ENST00000696273.1:c.461-3A>G ENSP00000512516.1:n.461-3A>G
ENST00000229335.11:c.428-3A>G MANE Select ENSP00000229335.6:n.428-3A>G
ENST00000229335.10:c.428-3A>G ENSP00000229335.6:n.428-3A>G
ENST00000537228.5:c.428-33A>G ENSP00000445691.1:n.428-33A>G
ENST00000543081.5:c.423+290A>G
ENST00000544516.5:c.153-588A>G
ENST00000545512.1:c.424-3A>G
ENST00000545576.1:n.751A>G
NM_020661.2:c.428-3A>G , LRG_17t1:c.428-3A>G NP_065712.1:n.428-3A>G
XM_011520772.1:c.428-33A>G XP_011519074.1:n.428-33A>G
XM_011520773.1:c.427+290A>G XP_011519075.1:n.427+290A>G
NM_001330343.1:c.428-33A>G NP_001317272.1:n.428-33A>G
NM_020661.3:c.428-3A>G NP_065712.1:n.428-3A>G
XM_011520773.2:c.427+290A>G XP_011519075.1:n.427+290A>G
NM_020661.4:c.428-3A>G MANE Select NP_065712.1:n.428-3A>G
NM_001330343.2:c.428-33A>G NP_001317272.1:n.428-33A>G