Canonical Allele Identifier: CA10633607

Gene: AICDA

Linked Data

• ClinVar Variation Id: 310567
• ClinVar RCV Id: RCV000346776
• dbSNP Id: rs74372815
• gnomAD v2: 12-8756162-G-T
• gnomAD v3: 12-8603566-G-T
• gnomAD v4: 12-8603566-G-T
• MyVariant Identifiers: chr12:g.8756162G>T (hg19) ; chr12:g.8603566G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8603566G>T , CM000674.2:g.8603566G>T	GRCh38
NC_000012.11:g.8756162G>T , CM000674.1:g.8756162G>T	GRCh37
NC_000012.10:g.8647429G>T	NCBI36
NG_011588.1:g.14281C>A , LRG_17:g.14281C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.*718C>A	ENSP00000445691.1:n.*718C>A
ENST00000543081.6:c.*761C>A	ENSP00000439103.2:n.*761C>A
ENST00000545576.2:n.1716C>A
ENST00000696246.1:c.*718C>A	ENSP00000512504.1:n.*718C>A
ENST00000696271.1:n.1727C>A
ENST00000696272.1:c.*718C>A	ENSP00000512515.1:n.*718C>A
ENST00000696273.1:c.*718C>A	ENSP00000512516.1:n.*718C>A
ENST00000229335.11:c.*718C>A MANE Select	ENSP00000229335.6:n.*718C>A
ENST00000229335.10:c.*718C>A	ENSP00000229335.6:n.*718C>A
NM_020661.2:c.*718C>A , LRG_17t1:c.*718C>A	NP_065712.1:n.*718C>A
XM_011520772.1:c.*718C>A	XP_011519074.1:n.*718C>A
NM_001330343.1:c.*718C>A	NP_001317272.1:n.*718C>A
NM_020661.3:c.*718C>A	NP_065712.1:n.*718C>A
NM_020661.4:c.*718C>A MANE Select	NP_065712.1:n.*718C>A
NM_001330343.2:c.*718C>A	NP_001317272.1:n.*718C>A