Canonical Allele Identifier: CA2015109959

Gene: AICDA

Linked Data

• dbSNP Id: rs1941256280

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604967G>C , CM000674.2:g.8604967G>C	GRCh38
NC_000012.11:g.8757563G>C , CM000674.1:g.8757563G>C	GRCh37
NC_000012.10:g.8648830G>C	NCBI36
NG_011588.1:g.12880C>G , LRG_17:g.12880C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.428-75C>G	ENSP00000445691.1:n.428-75C>G
ENST00000543081.6:c.427+248C>G	ENSP00000439103.2:n.427+248C>G
ENST00000544516.6:c.157-630C>G	ENSP00000439538.2:n.157-630C>G
ENST00000545576.2:n.784C>G
ENST00000696246.1:c.413-75C>G	ENSP00000512504.1:n.413-75C>G
ENST00000696271.1:n.795C>G
ENST00000696272.1:c.413-45C>G	ENSP00000512515.1:n.413-45C>G
ENST00000696273.1:c.461-45C>G	ENSP00000512516.1:n.461-45C>G
ENST00000229335.11:c.428-45C>G MANE Select	ENSP00000229335.6:n.428-45C>G
ENST00000229335.10:c.428-45C>G	ENSP00000229335.6:n.428-45C>G
ENST00000537228.5:c.428-75C>G	ENSP00000445691.1:n.428-75C>G
ENST00000543081.5:c.423+248C>G
ENST00000544516.5:c.153-630C>G
ENST00000545512.1:c.424-45C>G
ENST00000545576.1:n.709C>G
NM_020661.2:c.428-45C>G , LRG_17t1:c.428-45C>G	NP_065712.1:n.428-45C>G
XM_011520772.1:c.428-75C>G	XP_011519074.1:n.428-75C>G
XM_011520773.1:c.427+248C>G	XP_011519075.1:n.427+248C>G
NM_001330343.1:c.428-75C>G	NP_001317272.1:n.428-75C>G
NM_020661.3:c.428-45C>G	NP_065712.1:n.428-45C>G
XM_011520773.2:c.427+248C>G	XP_011519075.1:n.427+248C>G
NM_020661.4:c.428-45C>G MANE Select	NP_065712.1:n.428-45C>G
NM_001330343.2:c.428-75C>G	NP_001317272.1:n.428-75C>G