Canonical Allele Identifier: CA392299381

Gene: TRIM69

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44767673C>G , CM000677.2:g.44767673C>G	GRCh38
NC_000015.9:g.45059871C>G , CM000677.1:g.45059871C>G	GRCh37
NC_000015.8:g.42847163C>G	NCBI36
NG_033935.1:g.36312C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329464.9:c.1404C>G MANE Select	ENSP00000332284.3:p.Phe468Leu
ENST00000329464.8:c.1404C>G	ENSP00000332284.3:p.Phe468Leu
ENST00000338264.8:c.927C>G	ENSP00000342922.4:p.Phe309Leu
ENST00000558173.5:n.5537C>G
ENST00000558329.5:c.741C>G	ENSP00000453332.1:p.Phe247Leu
ENST00000559390.5:c.1404C>G	ENSP00000453177.1:p.Phe468Leu
ENST00000560442.5:c.792C>G	ENSP00000453549.1:p.Phe264Leu
ENST00000561043.5:c.693C>G	ENSP00000453077.1:p.Phe231Leu
NM_001301144.1:c.792C>G	NP_001288073.1:p.Phe264Leu
NM_001301145.1:c.741C>G	NP_001288074.1:p.Phe247Leu
NM_001301146.1:c.693C>G	NP_001288075.1:p.Phe231Leu
NM_080745.4:c.927C>G	NP_542783.2:p.Phe309Leu
NM_182985.4:c.1404C>G	NP_892030.3:p.Phe468Leu
NM_182985.5:c.1404C>G MANE Select	NP_892030.3:p.Phe468Leu
NM_001301144.2:c.792C>G	NP_001288073.1:p.Phe264Leu
NM_001301145.2:c.741C>G	NP_001288074.1:p.Phe247Leu
NM_001301146.2:c.693C>G	NP_001288075.1:p.Phe231Leu
NM_080745.5:c.927C>G	NP_542783.2:p.Phe309Leu