Canonical Allele Identifier: CA10643408

Gene: AICDA

Linked Data

• ClinVar Variation Id: 310553
• ClinVar RCV Id: RCV000365179
• dbSNP Id: rs886049868
• MyVariant Identifiers: chr12:g.8755618G>A (hg19) ; chr12:g.8603022G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8603022G>A , CM000674.2:g.8603022G>A	GRCh38
NC_000012.11:g.8755618G>A , CM000674.1:g.8755618G>A	GRCh37
NC_000012.10:g.8646885G>A	NCBI36
NG_011588.1:g.14825C>T , LRG_17:g.14825C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.*1262C>T	ENSP00000445691.1:n.*1262C>T
ENST00000543081.6:c.*1305C>T	ENSP00000439103.2:n.*1305C>T
ENST00000545576.2:n.2260C>T
ENST00000696246.1:c.*1262C>T	ENSP00000512504.1:n.*1262C>T
ENST00000696271.1:n.2271C>T
ENST00000696272.1:c.*1262C>T	ENSP00000512515.1:n.*1262C>T
ENST00000696273.1:c.*1262C>T	ENSP00000512516.1:n.*1262C>T
ENST00000229335.11:c.*1262C>T MANE Select	ENSP00000229335.6:n.*1262C>T
ENST00000229335.10:c.*1262C>T	ENSP00000229335.6:n.*1262C>T
NM_020661.2:c.*1262C>T , LRG_17t1:c.*1262C>T	NP_065712.1:n.*1262C>T
NM_001330343.1:c.*1262C>T	NP_001317272.1:n.*1262C>T
NM_020661.3:c.*1262C>T	NP_065712.1:n.*1262C>T
NM_020661.4:c.*1262C>T MANE Select	NP_065712.1:n.*1262C>T
NM_001330343.2:c.*1262C>T	NP_001317272.1:n.*1262C>T