Canonical Allele Identifier: CA1190159214

Gene: TRIM33

Linked Data

• dbSNP Id: rs1651492884
• gnomAD v4: 1-114395460-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114395460T>A , CM000663.2:g.114395460T>A	GRCh38
NC_000001.10:g.114938082T>A , CM000663.1:g.114938082T>A	GRCh37
NC_000001.9:g.114739605T>A	NCBI36
NG_023287.1:g.120700A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358465.7:c.*2188A>T MANE Select	ENSP00000351250.2:n.*2188A>T
ENST00000358465.6:c.*2188A>T	ENSP00000351250.2:n.*2188A>T
NM_015906.3:c.*2188A>T	NP_056990.3:n.*2188A>T
NM_033020.2:c.*2188A>T	NP_148980.2:n.*2188A>T
XM_005270936.2:c.*2188A>T	XP_005270993.1:n.*2188A>T
XM_005270937.2:c.*2188A>T	XP_005270994.1:n.*2188A>T
XM_011541568.1:c.*2188A>T	XP_011539870.1:n.*2188A>T
XM_005270936.4:c.*2188A>T	XP_005270993.1:n.*2188A>T
XM_005270937.4:c.*2188A>T	XP_005270994.1:n.*2188A>T
XM_011541568.3:c.*2188A>T	XP_011539870.1:n.*2188A>T
NM_015906.4:c.*2188A>T MANE Select	NP_056990.3:n.*2188A>T
NM_033020.3:c.*2188A>T	NP_148980.2:n.*2188A>T