Canonical Allele Identifier: CA5872953

Gene: TRIM66

Linked Data

• dbSNP Id: rs11042023
• ExAC: 11:8662516 T / C
• gnomAD v2: 11-8662516-T-C
• gnomAD v3: 11-8640969-T-C
• gnomAD v4: 11-8640969-T-C
• MyVariant Identifiers: chr11:g.8662516T>C (hg19) ; chr11:g.8640969T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8640969T>C , CM000673.2:g.8640969T>C	GRCh38
NC_000011.9:g.8662516T>C , CM000673.1:g.8662516T>C	GRCh37
NC_000011.8:g.8619092T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000525788.2:c.971A>G	ENSP00000516161.1:p.His324Arg
ENST00000705689.1:c.1295A>G	ENSP00000516162.1:p.His432Arg
ENST00000705690.1:c.971A>G	ENSP00000516163.1:p.His324Arg
ENST00000705691.1:n.2341A>G
ENST00000402157.7:c.1406A>G
ENST00000646038.2:c.1406A>G MANE Select	ENSP00000495413.1:p.His469Arg
ENST00000646038.1:c.1406A>G	ENSP00000495413.1:p.His469Arg
ENST00000299550.10:c.971A>G	ENSP00000299550.6:p.His324Arg
ENST00000402157.6:c.965A>G	ENSP00000384876.2:p.His322Arg
ENST00000481014.6:n.1166A>G
NM_014818.1:c.971A>G	NP_055633.1:p.His324Arg
XM_006718397.2:c.1406A>G	XP_006718460.1:p.His469Arg
XM_006718398.2:c.971A>G	XP_006718461.1:p.His324Arg
XM_011520504.1:c.1406A>G	XP_011518806.1:p.His469Arg
XM_011520505.1:c.1406A>G	XP_011518807.1:p.His469Arg
XM_011520506.1:c.1406A>G	XP_011518808.1:p.His469Arg
XM_011520507.1:c.1406A>G	XP_011518809.1:p.His469Arg
XM_011520508.1:c.1406A>G	XP_011518810.1:p.His469Arg
XM_011520509.1:c.1406A>G	XP_011518811.1:p.His469Arg
XM_011520510.1:c.1406A>G	XP_011518812.1:p.His469Arg
XM_011520511.1:c.1295A>G	XP_011518813.1:p.His432Arg
XM_011520512.1:c.1148A>G	XP_011518814.1:p.His383Arg
XM_011520513.1:c.1148A>G	XP_011518815.1:p.His383Arg
XM_011520514.1:c.1148A>G	XP_011518816.1:p.His383Arg
XM_011520515.1:c.971A>G	XP_011518817.1:p.His324Arg
XM_011520516.1:c.971A>G	XP_011518818.1:p.His324Arg
XM_011520517.1:c.971A>G	XP_011518819.1:p.His324Arg
XM_011520518.1:c.971A>G	XP_011518820.1:p.His324Arg
XM_011520519.1:c.971A>G	XP_011518821.1:p.His324Arg
XM_011520520.1:c.971A>G	XP_011518822.1:p.His324Arg
XM_011520521.1:c.971A>G	XP_011518823.1:p.His324Arg
XM_011520522.1:c.971A>G	XP_011518824.1:p.His324Arg
XM_011520523.1:c.971A>G	XP_011518825.1:p.His324Arg
XM_011520524.1:c.1406A>G	XP_011518826.1:p.His469Arg
XM_011520525.1:c.1406A>G	XP_011518827.1:p.His469Arg
XM_011520526.1:c.233A>G	XP_011518828.1:p.His78Arg
XM_011520527.1:c.-54-488A>G	XP_011518829.1:n.-54-488A>G
XR_930929.1:n.2011A>G
XR_930930.1:n.2011A>G
XR_930931.1:n.2011A>G
XM_006718398.3:c.971A>G	XP_006718461.1:p.His324Arg
XM_011520507.3:c.1406A>G	XP_011518809.1:p.His469Arg
XM_011520508.2:c.1406A>G	XP_011518810.1:p.His469Arg
XM_011520514.2:c.1148A>G	XP_011518816.1:p.His383Arg
XM_011520517.2:c.971A>G	XP_011518819.1:p.His324Arg
XM_011520522.2:c.971A>G	XP_011518824.1:p.His324Arg
XM_011520523.2:c.971A>G	XP_011518825.1:p.His324Arg
XM_011520526.2:c.233A>G	XP_011518828.1:p.His78Arg
XM_017018629.1:c.1406A>G	XP_016874118.1:p.His469Arg
XM_017018630.1:c.1148A>G	XP_016874119.1:p.His383Arg
XM_017018631.1:c.971A>G	XP_016874120.1:p.His324Arg
NM_001388022.1:c.1406A>G MANE Select	NP_001374951.1:p.His469Arg
NM_001388023.1:c.1295A>G	NP_001374952.1:p.His432Arg
NM_001388024.1:c.1406A>G	NP_001374953.1:p.His469Arg
NM_014818.2:c.971A>G	NP_055633.1:p.His324Arg