Canonical Allele Identifier: CA8664154
Gene: TRIM25 HGNC NCBI
COSMIC:
COSM4000224 (not active)
MyVariant.info:
GRCh38 chr17:g.56901433G>A
GRCh37 chr17:g.54978794G>A
Revel Score:
ENST00000316881 (MANE Select) 0.047
ENST00000537230 0.047
gnomAD v2:
17:54978794 G / A
gnomAD v3:
17:56901433 G / A
gnomAD v4:
chr17-56901433-G-A
Joint Max Group AF 0.81433671 (AFR)
Genomes Max Group AF 0.81234883 (AFR)
Exomes Max Group AF 0.8117963 (AFR)
dbSNP:
205498
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56901433G>A , CM000679.2:g.56901433G>A GRCh38
NC_000017.10:g.54978794G>A , CM000679.1:g.54978794G>A GRCh37
NC_000017.9:g.52333793G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000537230.3:c.1073C>T ENSP00000445961.1:p.Pro358Leu
ENST00000572021.6:c.*486C>T ENSP00000459980.2:n.*486C>T
ENST00000682509.1:n.343C>T
ENST00000682766.1:c.1073C>T ENSP00000507876.1:p.Pro358Leu
ENST00000316881.9:c.1073C>T MANE Select ENSP00000323889.4:p.Pro358Leu
ENST00000648772.1:c.1073C>T ENSP00000498158.1:p.Pro358Leu
ENST00000316881.8:c.1073C>T ENSP00000323889.4:p.Pro358Leu
ENST00000537230.2:c.1073C>T ENSP00000445961.1:p.Pro358Leu
ENST00000570473.5:n.235C>T
ENST00000570749.5:n.380C>T
ENST00000572021.5:c.618C>T ENSP00000459980.1:n.618C>T
ENST00000572550.1:n.513C>T
NM_005082.4:c.1073C>T NP_005073.2:p.Pro358Leu
NM_005082.5:c.1073C>T MANE Select NP_005073.2:p.Pro358Leu
Search 100 bp 5'
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