Canonical Allele Identifier: CA2559579724
Gene: TRIM33 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114395454_114395458del , CM000663.2:g.114395454_114395458del GRCh38
NC_000001.10:g.114938076_114938080del , CM000663.1:g.114938076_114938080del GRCh37
NC_000001.9:g.114739599_114739603del NCBI36
NG_023287.1:g.120702_120706del

Transcript Alleles

HGVS Amino-acid Change
ENST00000358465.7:c.*2190_*2194del MANE Select ENSP00000351250.2:n.*2190_*2194del
ENST00000358465.6:c.*2190_*2194del ENSP00000351250.2:n.*2190_*2194del
NM_015906.3:c.*2190_*2194del NP_056990.3:n.*2190_*2194del
NM_033020.2:c.*2190_*2194del NP_148980.2:n.*2190_*2194del
XM_005270936.2:c.*2190_*2194del XP_005270993.1:n.*2190_*2194del
XM_005270937.2:c.*2190_*2194del XP_005270994.1:n.*2190_*2194del
XM_011541568.1:c.*2190_*2194del XP_011539870.1:n.*2190_*2194del
XM_005270936.4:c.*2190_*2194del XP_005270993.1:n.*2190_*2194del
XM_005270937.4:c.*2190_*2194del XP_005270994.1:n.*2190_*2194del
XM_011541568.3:c.*2190_*2194del XP_011539870.1:n.*2190_*2194del
NM_015906.4:c.*2190_*2194del MANE Select NP_056990.3:n.*2190_*2194del
NM_033020.3:c.*2190_*2194del NP_148980.2:n.*2190_*2194del
Search 100 bp 5'
Search 100 bp 3'