Canonical Allele Identifier: CA399922065

Gene: TRIM25

Linked Data

• ClinVar Variation Id: 2338564
• ClinVar RCV Id: RCV004180421
• dbSNP Id: rs1368290262
• MyVariant Identifiers: chr17:g.54969173G>A (hg19) ; chr17:g.56891812G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56891812G>A , CM000679.2:g.56891812G>A	GRCh38
NC_000017.10:g.54969173G>A , CM000679.1:g.54969173G>A	GRCh37
NC_000017.9:g.52324172G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537230.3:c.1781C>T	ENSP00000445961.1:p.Ala594Val
ENST00000572021.6:c.*1194C>T	ENSP00000459980.2:n.*1194C>T
ENST00000682766.1:c.1363+3531C>T	ENSP00000507876.1:n.1363+3531C>T
ENST00000316881.9:c.1781C>T MANE Select	ENSP00000323889.4:p.Ala594Val
ENST00000648772.1:c.1363+3531C>T	ENSP00000498158.1:n.1363+3531C>T
ENST00000316881.8:c.1781C>T	ENSP00000323889.4:p.Ala594Val
ENST00000537230.2:c.1781C>T	ENSP00000445961.1:p.Ala594Val
ENST00000572021.5:c.1326C>T	ENSP00000459980.1:n.1326C>T
NM_005082.4:c.1781C>T	NP_005073.2:p.Ala594Val
NM_005082.5:c.1781C>T MANE Select	NP_005073.2:p.Ala594Val