Canonical Allele Identifier: CA14423045
Gene: TRIM25 HGNC NCBI

Linked Data

dbSNP Id: rs205499

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56895040G>A , CM000679.2:g.56895040G>A GRCh38
NC_000017.10:g.54972401G>A , CM000679.1:g.54972401G>A GRCh37
NC_000017.9:g.52327400G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000537230.3:c.1363+303C>T ENSP00000445961.1:n.1363+303C>T
ENST00000572021.6:c.*776+303C>T ENSP00000459980.2:n.*776+303C>T
ENST00000682766.1:c.1363+303C>T ENSP00000507876.1:n.1363+303C>T
ENST00000316881.9:c.1363+303C>T MANE Select ENSP00000323889.4:n.1363+303C>T
ENST00000648772.1:c.1363+303C>T ENSP00000498158.1:n.1363+303C>T
ENST00000316881.8:c.1363+303C>T ENSP00000323889.4:n.1363+303C>T
ENST00000537230.2:c.1363+303C>T ENSP00000445961.1:n.1363+303C>T
ENST00000572021.5:c.908+303C>T ENSP00000459980.1:n.908+303C>T
ENST00000574234.1:n.353+303C>T
NM_005082.4:c.1363+303C>T NP_005073.2:n.1363+303C>T
NM_005082.5:c.1363+303C>T MANE Select NP_005073.2:n.1363+303C>T