Canonical Allele Identifier: CA1005997932

Gene: TRIM33

Linked Data

• dbSNP Id: rs1651494870
• gnomAD v3: 1-114395494-A-C
• gnomAD v4: 1-114395494-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114395494A>C , CM000663.2:g.114395494A>C	GRCh38
NC_000001.10:g.114938116A>C , CM000663.1:g.114938116A>C	GRCh37
NC_000001.9:g.114739639A>C	NCBI36
NG_023287.1:g.120666T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000358465.7:c.*2154T>G MANE Select	ENSP00000351250.2:n.*2154T>G
ENST00000358465.6:c.*2154T>G	ENSP00000351250.2:n.*2154T>G
NM_015906.3:c.*2154T>G	NP_056990.3:n.*2154T>G
NM_033020.2:c.*2154T>G	NP_148980.2:n.*2154T>G
XM_005270936.2:c.*2154T>G	XP_005270993.1:n.*2154T>G
XM_005270937.2:c.*2154T>G	XP_005270994.1:n.*2154T>G
XM_011541568.1:c.*2154T>G	XP_011539870.1:n.*2154T>G
XM_005270936.4:c.*2154T>G	XP_005270993.1:n.*2154T>G
XM_005270937.4:c.*2154T>G	XP_005270994.1:n.*2154T>G
XM_011541568.3:c.*2154T>G	XP_011539870.1:n.*2154T>G
NM_015906.4:c.*2154T>G MANE Select	NP_056990.3:n.*2154T>G
NM_033020.3:c.*2154T>G	NP_148980.2:n.*2154T>G