Canonical Allele Identifier: CA2745126156

Gene: TRIM33

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114395466C>A , CM000663.2:g.114395466C>A	GRCh38
NC_000001.10:g.114938088C>A , CM000663.1:g.114938088C>A	GRCh37
NC_000001.9:g.114739611C>A	NCBI36
NG_023287.1:g.120694G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358465.7:c.*2182G>T MANE Select	ENSP00000351250.2:n.*2182G>T
ENST00000358465.6:c.*2182G>T	ENSP00000351250.2:n.*2182G>T
NM_015906.3:c.*2182G>T	NP_056990.3:n.*2182G>T
NM_033020.2:c.*2182G>T	NP_148980.2:n.*2182G>T
XM_005270936.2:c.*2182G>T	XP_005270993.1:n.*2182G>T
XM_005270937.2:c.*2182G>T	XP_005270994.1:n.*2182G>T
XM_011541568.1:c.*2182G>T	XP_011539870.1:n.*2182G>T
XM_005270936.4:c.*2182G>T	XP_005270993.1:n.*2182G>T
XM_005270937.4:c.*2182G>T	XP_005270994.1:n.*2182G>T
XM_011541568.3:c.*2182G>T	XP_011539870.1:n.*2182G>T
NM_015906.4:c.*2182G>T MANE Select	NP_056990.3:n.*2182G>T
NM_033020.3:c.*2182G>T	NP_148980.2:n.*2182G>T