Canonical Allele Identifier: CA2534314473
Gene: TRIM33 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114395470T>G , CM000663.2:g.114395470T>G GRCh38
NC_000001.10:g.114938092T>G , CM000663.1:g.114938092T>G GRCh37
NC_000001.9:g.114739615T>G NCBI36
NG_023287.1:g.120690A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358465.7:c.*2178A>C MANE Select ENSP00000351250.2:n.*2178A>C
ENST00000358465.6:c.*2178A>C ENSP00000351250.2:n.*2178A>C
NM_015906.3:c.*2178A>C NP_056990.3:n.*2178A>C
NM_033020.2:c.*2178A>C NP_148980.2:n.*2178A>C
XM_005270936.2:c.*2178A>C XP_005270993.1:n.*2178A>C
XM_005270937.2:c.*2178A>C XP_005270994.1:n.*2178A>C
XM_011541568.1:c.*2178A>C XP_011539870.1:n.*2178A>C
XM_005270936.4:c.*2178A>C XP_005270993.1:n.*2178A>C
XM_005270937.4:c.*2178A>C XP_005270994.1:n.*2178A>C
XM_011541568.3:c.*2178A>C XP_011539870.1:n.*2178A>C
NM_015906.4:c.*2178A>C MANE Select NP_056990.3:n.*2178A>C
NM_033020.3:c.*2178A>C NP_148980.2:n.*2178A>C
Search 100 bp 5'
Search 100 bp 3'