Canonical Allele Identifier: CA5845726

Gene: TRIM22 TRIM5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5696440C>A , CM000673.2:g.5696440C>A	GRCh38
NC_000011.9:g.5717670C>A , CM000673.1:g.5717670C>A	GRCh37
NC_000011.8:g.5674246C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006074.5:c.208C>A (TRIM22) MANE Select	NP_006065.2:p.Pro70Thr
ENST00000379965.8:c.208C>A (TRIM22) MANE Select	ENSP00000369299.3:p.Pro70Thr
NM_001199573.1:c.208C>A (TRIM22)	NP_001186502.1:p.Pro70Thr
NM_001199573.2:c.208C>A (TRIM22)	NP_001186502.1:p.Pro70Thr
NM_006074.4:c.208C>A (TRIM22)	NP_006065.2:p.Pro70Thr
ENST00000379965.7:c.208C>A (TRIM22)	ENSP00000369299.3:p.Pro70Thr
ENST00000380027.5:c.-440-11046G>T (TRIM5)	ENSP00000369366.1:n.-440-11046G>T
ENST00000412903.1:c.-61-16202G>T (TRIM5)	ENSP00000388031.1:n.-61-16202G>T
ENST00000414641.5:c.208C>A (TRIM22)	ENSP00000396849.1:p.Pro70Thr
ENST00000425490.5:c.208C>A (TRIM22)	ENSP00000400417.1:p.Pro70Thr
ENST00000454828.5:c.208C>A (TRIM22)	ENSP00000393250.1:p.Pro70Thr
ENST00000454828.6:c.208C>A (TRIM22)	ENSP00000393250.2:p.Pro70Thr
ENST00000460454.1:n.353C>A (TRIM22)
ENST00000460454.2:n.564C>A (TRIM22)
ENST00000480395.6:n.407C>A (TRIM22)
ENST00000699052.1:n.511C>A (TRIM22)
ENST00000699053.1:c.208C>A (TRIM22)	ENSP00000514103.1:p.Pro70Thr
ENST00000699054.1:n.407C>A (TRIM22)
ENST00000699055.1:n.368C>A (TRIM22)
ENST00000699056.1:n.368C>A (TRIM22)