Canonical Allele Identifier: CA15694082
Gene: TRIM22 HGNC NCBI
TRIM5 HGNC NCBI

Linked Data

dbSNP Id: rs2291841
gnomAD v2: 11-5710896-A-C
gnomAD v3: 11-5689666-A-C
gnomAD v4: 11-5689666-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5689666A>C , CM000673.2:g.5689666A>C GRCh38
NC_000011.9:g.5710896A>C , CM000673.1:g.5710896A>C GRCh37
NC_000011.8:g.5667472A>C NCBI36
NG_029122.1:g.444T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000460454.2:n.57A>C (TRIM22)
ENST00000699052.1:n.4A>C (TRIM22)
ENST00000380027.5:c.-440-4272T>G (TRIM5) ENSP00000369366.1:n.-440-4272T>G
ENST00000412903.1:c.-61-9428T>G (TRIM5) ENSP00000388031.1:n.-61-9428T>G
NM_001199573.1:c.-300A>C (TRIM22) NP_001186502.1:n.-300A>C
NM_006074.4:c.-300A>C (TRIM22) NP_006065.2:n.-300A>C