Canonical Allele Identifier: CA752039880

Gene: TFIP11

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26503508T>A , CM000684.2:g.26503508T>A	GRCh38
NC_000022.10:g.26899474T>A , CM000684.1:g.26899474T>A	GRCh37
NC_000022.9:g.25229474T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407690.6:c.648+158A>T MANE Select	ENSP00000384421.1:n.648+158A>T
ENST00000405938.5:c.648+158A>T	ENSP00000384297.1:n.648+158A>T
ENST00000407148.5:c.648+158A>T	ENSP00000385861.1:n.648+158A>T
ENST00000407431.5:c.648+158A>T	ENSP00000383892.1:n.648+158A>T
ENST00000407690.5:c.648+158A>T	ENSP00000384421.1:n.648+158A>T
ENST00000450493.1:c.158+158A>T
ENST00000493698.1:n.538+158A>T
ENST00000496523.5:n.324+158A>T
ENST00000619735.4:c.648+158A>T	ENSP00000480171.1:n.648+158A>T
NM_001008697.1:c.648+158A>T	NP_001008697.1:n.648+158A>T
NM_012143.2:c.648+158A>T	NP_036275.1:n.648+158A>T
XM_011530079.1:c.648+158A>T	XP_011528381.1:n.648+158A>T
NM_001008697.2:c.648+158A>T	NP_001008697.1:n.648+158A>T
NM_001346857.1:c.648+158A>T	NP_001333786.1:n.648+158A>T
NM_001346858.1:c.648+158A>T	NP_001333787.1:n.648+158A>T
NM_001346859.1:c.648+158A>T	NP_001333788.1:n.648+158A>T
NM_001346861.1:c.648+158A>T	NP_001333790.1:n.648+158A>T
NM_001346862.1:c.555+158A>T	NP_001333791.1:n.555+158A>T
NM_012143.3:c.648+158A>T	NP_036275.1:n.648+158A>T
XM_024452194.1:c.648+158A>T	XP_024307962.1:n.648+158A>T
XM_024452195.1:c.648+158A>T	XP_024307963.1:n.648+158A>T
NM_012143.4:c.648+158A>T MANE Select	NP_036275.1:n.648+158A>T
NM_001008697.3:c.648+158A>T	NP_001008697.1:n.648+158A>T
NM_001346857.2:c.648+158A>T	NP_001333786.1:n.648+158A>T
NM_001346858.2:c.648+158A>T	NP_001333787.1:n.648+158A>T
NM_001346859.2:c.648+158A>T	NP_001333788.1:n.648+158A>T
NM_001346861.2:c.648+158A>T	NP_001333790.1:n.648+158A>T
NM_001346862.2:c.555+158A>T	NP_001333791.1:n.555+158A>T