Canonical Allele Identifier: CA11546075

Gene: TFDP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142088295C>A , CM000665.2:g.142088295C>A	GRCh38
NC_000003.11:g.141807137C>A , CM000665.1:g.141807137C>A	GRCh37
NC_000003.10:g.143289827C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489671.6:c.82+4766G>T MANE Select	ENSP00000420616.1:n.82+4766G>T
ENST00000464782.5:n.356-34146G>T
ENST00000467072.5:c.-137+4766G>T	ENSP00000418590.1:n.-137+4766G>T
ENST00000467634.1:c.82+4766G>T	ENSP00000419540.1:n.82+4766G>T
ENST00000475734.5:c.-102+60888G>T	ENSP00000417108.1:n.-102+60888G>T
ENST00000476617.5:n.462+4766G>T
ENST00000487734.5:c.82+4766G>T	ENSP00000417384.1:n.82+4766G>T
ENST00000488107.6:c.-102+2497G>T	ENSP00000420456.2:n.-102+2497G>T
ENST00000489671.5:c.82+4766G>T	ENSP00000420616.1:n.82+4766G>T
ENST00000494358.5:c.-102+13440G>T	ENSP00000420657.1:n.-102+13440G>T
ENST00000495095.6:n.529+4766G>T
NM_001178138.1:c.-137+4766G>T	NP_001171609.1:n.-137+4766G>T
NM_001178139.1:c.82+4766G>T	NP_001171610.1:n.82+4766G>T
XM_005247731.1:c.82+4766G>T	XP_005247788.1:n.82+4766G>T
XM_011513101.1:c.-88+4766G>T	XP_011511403.1:n.-88+4766G>T
XM_011513103.1:c.-123+4766G>T	XP_011511405.1:n.-123+4766G>T
XM_011513106.1:c.-88+4766G>T	XP_011511408.1:n.-88+4766G>T
XM_011513107.1:c.82+4766G>T	XP_011511409.1:n.82+4766G>T
XM_011513108.1:c.-88+4766G>T	XP_011511410.1:n.-88+4766G>T
XM_011513110.1:c.-123+4766G>T	XP_011511412.1:n.-123+4766G>T
XM_005247731.3:c.82+4766G>T	XP_005247788.1:n.82+4766G>T
XM_011513101.3:c.-88+4766G>T	XP_011511403.1:n.-88+4766G>T
XM_011513106.3:c.-88+4766G>T	XP_011511408.1:n.-88+4766G>T
XM_011513107.2:c.82+4766G>T	XP_011511409.1:n.82+4766G>T
XM_011513108.3:c.-88+4766G>T	XP_011511410.1:n.-88+4766G>T
XM_017007091.1:c.82+4766G>T	XP_016862580.1:n.82+4766G>T
XM_017007097.2:c.-137+4766G>T	XP_016862586.1:n.-137+4766G>T
XM_017007098.2:c.-326+4766G>T	XP_016862587.1:n.-326+4766G>T
XM_017007100.2:c.82+4766G>T	XP_016862589.1:n.82+4766G>T
XM_017007102.2:c.-88+4766G>T	XP_016862591.1:n.-88+4766G>T
XM_017007104.2:c.-88+4766G>T	XP_016862593.1:n.-88+4766G>T
XM_024453726.1:c.-123+4766G>T	XP_024309494.1:n.-123+4766G>T
XM_024453728.1:c.-123+4766G>T	XP_024309496.1:n.-123+4766G>T
XM_024453730.1:c.-123+4766G>T	XP_024309498.1:n.-123+4766G>T
NM_001178138.2:c.-137+4766G>T	NP_001171609.1:n.-137+4766G>T
NM_001178139.2:c.82+4766G>T MANE Select	NP_001171610.1:n.82+4766G>T
NM_001375773.1:c.82+4766G>T	NP_001362702.1:n.82+4766G>T
NM_001375775.1:c.-88+4766G>T	NP_001362704.1:n.-88+4766G>T
NM_001375776.1:c.-326+4766G>T	NP_001362705.1:n.-326+4766G>T
NM_001375778.1:c.-137+4766G>T	NP_001362707.1:n.-137+4766G>T
NM_001375780.1:c.-88+4766G>T	NP_001362709.1:n.-88+4766G>T