Canonical Allele Identifier: CA692859088

Gene: AICDA

Linked Data

• dbSNP Id: rs1441139336
• gnomAD v4: 12-8604661-A-G
• MyVariant Identifiers: chr12:g.8757257A>G (hg19) ; chr12:g.8604661A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604661A>G , CM000674.2:g.8604661A>G	GRCh38
NC_000012.11:g.8757257A>G , CM000674.1:g.8757257A>G	GRCh37
NC_000012.10:g.8648524A>G	NCBI36
NG_011588.1:g.13186T>C , LRG_17:g.13186T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.513+146T>C	ENSP00000445691.1:n.513+146T>C
ENST00000543081.6:c.428-324T>C	ENSP00000439103.2:n.428-324T>C
ENST00000544516.6:c.157-324T>C	ENSP00000439538.2:n.157-324T>C
ENST00000545576.2:n.944+146T>C
ENST00000696246.1:c.498+146T>C	ENSP00000512504.1:n.498+146T>C
ENST00000696271.1:n.955+146T>C
ENST00000696272.1:c.528+146T>C	ENSP00000512515.1:n.528+146T>C
ENST00000696273.1:c.576+146T>C	ENSP00000512516.1:n.576+146T>C
ENST00000229335.11:c.543+146T>C MANE Select	ENSP00000229335.6:n.543+146T>C
ENST00000229335.10:c.543+146T>C	ENSP00000229335.6:n.543+146T>C
ENST00000537228.5:c.513+146T>C	ENSP00000445691.1:n.513+146T>C
ENST00000543081.5:c.424-324T>C
ENST00000544516.5:c.153-324T>C
ENST00000545512.1:c.539+146T>C
ENST00000545576.1:n.869+146T>C
NM_020661.2:c.543+146T>C , LRG_17t1:c.543+146T>C	NP_065712.1:n.543+146T>C
XM_011520772.1:c.513+146T>C	XP_011519074.1:n.513+146T>C
XM_011520773.1:c.428-324T>C	XP_011519075.1:n.428-324T>C
NM_001330343.1:c.513+146T>C	NP_001317272.1:n.513+146T>C
NM_020661.3:c.543+146T>C	NP_065712.1:n.543+146T>C
XM_011520773.2:c.428-324T>C	XP_011519075.1:n.428-324T>C
NM_020661.4:c.543+146T>C MANE Select	NP_065712.1:n.543+146T>C
NM_001330343.2:c.513+146T>C	NP_001317272.1:n.513+146T>C