Canonical Allele Identifier: CA2647232268

Gene: TRIM33

Linked Data

• gnomAD v4: 1-114395490-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114395490G>T , CM000663.2:g.114395490G>T	GRCh38
NC_000001.10:g.114938112G>T , CM000663.1:g.114938112G>T	GRCh37
NC_000001.9:g.114739635G>T	NCBI36
NG_023287.1:g.120670C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000358465.7:c.*2158C>A MANE Select	ENSP00000351250.2:n.*2158C>A
ENST00000358465.6:c.*2158C>A	ENSP00000351250.2:n.*2158C>A
NM_015906.3:c.*2158C>A	NP_056990.3:n.*2158C>A
NM_033020.2:c.*2158C>A	NP_148980.2:n.*2158C>A
XM_005270936.2:c.*2158C>A	XP_005270993.1:n.*2158C>A
XM_005270937.2:c.*2158C>A	XP_005270994.1:n.*2158C>A
XM_011541568.1:c.*2158C>A	XP_011539870.1:n.*2158C>A
XM_005270936.4:c.*2158C>A	XP_005270993.1:n.*2158C>A
XM_005270937.4:c.*2158C>A	XP_005270994.1:n.*2158C>A
XM_011541568.3:c.*2158C>A	XP_011539870.1:n.*2158C>A
NM_015906.4:c.*2158C>A MANE Select	NP_056990.3:n.*2158C>A
NM_033020.3:c.*2158C>A	NP_148980.2:n.*2158C>A