Canonical Allele Identifier: CA603209631

Gene: AICDA

Linked Data

• dbSNP Id: rs1450618632
• gnomAD v2: 12-8757235-C-G
• gnomAD v3: 12-8604639-C-G
• gnomAD v4: 12-8604639-C-G
• MyVariant Identifiers: chr12:g.8757235C>G (hg19) ; chr12:g.8604639C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604639C>G , CM000674.2:g.8604639C>G	GRCh38
NC_000012.11:g.8757235C>G , CM000674.1:g.8757235C>G	GRCh37
NC_000012.10:g.8648502C>G	NCBI36
NG_011588.1:g.13208G>C , LRG_17:g.13208G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.513+168G>C	ENSP00000445691.1:n.513+168G>C
ENST00000543081.6:c.428-302G>C	ENSP00000439103.2:n.428-302G>C
ENST00000544516.6:c.157-302G>C	ENSP00000439538.2:n.157-302G>C
ENST00000545576.2:n.944+168G>C
ENST00000696246.1:c.498+168G>C	ENSP00000512504.1:n.498+168G>C
ENST00000696271.1:n.955+168G>C
ENST00000696272.1:c.528+168G>C	ENSP00000512515.1:n.528+168G>C
ENST00000696273.1:c.576+168G>C	ENSP00000512516.1:n.576+168G>C
ENST00000229335.11:c.543+168G>C MANE Select	ENSP00000229335.6:n.543+168G>C
ENST00000229335.10:c.543+168G>C	ENSP00000229335.6:n.543+168G>C
ENST00000537228.5:c.513+168G>C	ENSP00000445691.1:n.513+168G>C
ENST00000543081.5:c.424-302G>C
ENST00000544516.5:c.153-302G>C
ENST00000545512.1:c.539+168G>C
ENST00000545576.1:n.869+168G>C
NM_020661.2:c.543+168G>C , LRG_17t1:c.543+168G>C	NP_065712.1:n.543+168G>C
XM_011520772.1:c.513+168G>C	XP_011519074.1:n.513+168G>C
XM_011520773.1:c.428-302G>C	XP_011519075.1:n.428-302G>C
NM_001330343.1:c.513+168G>C	NP_001317272.1:n.513+168G>C
NM_020661.3:c.543+168G>C	NP_065712.1:n.543+168G>C
XM_011520773.2:c.428-302G>C	XP_011519075.1:n.428-302G>C
NM_020661.4:c.543+168G>C MANE Select	NP_065712.1:n.543+168G>C
NM_001330343.2:c.513+168G>C	NP_001317272.1:n.513+168G>C