Canonical Allele Identifier: CA2516801586
Gene: TRIM33 HGNC NCBI

Linked Data

dbSNP Id: rs60897900
gnomAD v4: 1-114395468-AT-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114395475del , CM000663.2:g.114395475del GRCh38
NC_000001.10:g.114938097del , CM000663.1:g.114938097del GRCh37
NC_000001.9:g.114739620del NCBI36
NG_023287.1:g.120691del

Transcript Alleles

HGVS Amino-acid change
ENST00000358465.7:c.*2179del MANE Select ENSP00000351250.2:n.*2179del
ENST00000358465.6:c.*2179del ENSP00000351250.2:n.*2179del
NM_015906.3:c.*2179del NP_056990.3:n.*2179del
NM_033020.2:c.*2179del NP_148980.2:n.*2179del
XM_005270936.2:c.*2179del XP_005270993.1:n.*2179del
XM_005270937.2:c.*2179del XP_005270994.1:n.*2179del
XM_011541568.1:c.*2179del XP_011539870.1:n.*2179del
XM_005270936.4:c.*2179del XP_005270993.1:n.*2179del
XM_005270937.4:c.*2179del XP_005270994.1:n.*2179del
XM_011541568.3:c.*2179del XP_011539870.1:n.*2179del
NM_015906.4:c.*2179del MANE Select NP_056990.3:n.*2179del
NM_033020.3:c.*2179del NP_148980.2:n.*2179del
Search 100 bp 5'
Search 100 bp 3'