Canonical Allele Identifier: CA2153776084

Gene: TTC8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88870247_88870248delinsTA , CM000676.2:g.88870247_88870248delinsTA	GRCh38
NC_000014.8:g.89336591_89336592delinsTA , CM000676.1:g.89336591_89336592delinsTA	GRCh37
NC_000014.7:g.88406344_88406345delinsTA	NCBI36
NG_008126.1:g.50614_50615delinsTA
NG_008126.2:g.51095_51096delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380656.7:c.1049+49_1049+50delinsTA MANE Select	ENSP00000370031.2:n.1049+49_1049+50delinsTA
ENST00000557580.3:c.414+49_414+50delinsTA	ENSP00000451955.2:n.414+49_414+50delinsTA
ENST00000338104.10:c.1097+49_1097+50delinsTA	ENSP00000337653.6:n.1097+49_1097+50delinsTA
ENST00000345383.9:c.1049+49_1049+50delinsTA	ENSP00000339486.6:n.1049+49_1049+50delinsTA
ENST00000346301.8:c.929+49_929+50delinsTA	ENSP00000298324.6:n.929+49_929+50delinsTA
ENST00000354441.10:c.254+49_254+50delinsTA	ENSP00000346427.6:n.254+49_254+50delinsTA
ENST00000358622.9:c.455+49_455+50delinsTA	ENSP00000351439.5:n.455+49_455+50delinsTA
ENST00000380656.6:c.1049+49_1049+50delinsTA	ENSP00000370031.2:n.1049+49_1049+50delinsTA
ENST00000536576.5:c.929+49_929+50delinsTA	ENSP00000445067.2:n.929+49_929+50delinsTA
ENST00000554686.5:c.898+49_898+50delinsTA
ENST00000555057.5:c.*456+49_*456+50delinsTA	ENSP00000450951.1:n.*456+49_*456+50delinsTA
ENST00000557580.2:c.414+49_414+50delinsTA
ENST00000614125.4:c.1097+49_1097+50delinsTA	ENSP00000482306.1:n.1097+49_1097+50delinsTA
ENST00000622513.4:c.1019+49_1019+50delinsTA	ENSP00000482721.1:n.1019+49_1019+50delinsTA
NM_001288781.1:c.1097+49_1097+50delinsTA	NP_001275710.1:n.1097+49_1097+50delinsTA
NM_001288782.1:c.455+49_455+50delinsTA	NP_001275711.1:n.455+49_455+50delinsTA
NM_001288783.1:c.332+49_332+50delinsTA	NP_001275712.1:n.332+49_332+50delinsTA
NM_144596.3:c.1049+49_1049+50delinsTA	NP_653197.2:n.1049+49_1049+50delinsTA
NM_198309.3:c.1019+49_1019+50delinsTA	NP_938051.1:n.1019+49_1019+50delinsTA
NM_198310.3:c.929+49_929+50delinsTA	NP_938052.1:n.929+49_929+50delinsTA
XM_006720035.1:c.1019+49_1019+50delinsTA	XP_006720098.1:n.1019+49_1019+50delinsTA
XM_006720037.2:c.929+49_929+50delinsTA	XP_006720100.1:n.929+49_929+50delinsTA
XM_011536432.1:c.1097+49_1097+50delinsTA	XP_011534734.1:n.1097+49_1097+50delinsTA
XM_011536433.1:c.1097+49_1097+50delinsTA	XP_011534735.1:n.1097+49_1097+50delinsTA
XM_011536434.1:c.1007+49_1007+50delinsTA	XP_011534736.1:n.1007+49_1007+50delinsTA
XM_011536435.1:c.332+49_332+50delinsTA	XP_011534737.1:n.332+49_332+50delinsTA
NM_001366535.1:c.1019+49_1019+50delinsTA	NP_001353464.1:n.1019+49_1019+50delinsTA
NM_001366536.1:c.929+49_929+50delinsTA	NP_001353465.1:n.929+49_929+50delinsTA
NR_159362.1:n.1136+49_1136+50delinsTA
XM_011536433.2:c.1097+49_1097+50delinsTA	XP_011534735.1:n.1097+49_1097+50delinsTA
XM_011536434.2:c.1007+49_1007+50delinsTA	XP_011534736.1:n.1007+49_1007+50delinsTA
XM_024449477.1:c.332+49_332+50delinsTA	XP_024305245.1:n.332+49_332+50delinsTA
NM_001366535.2:c.1019+49_1019+50delinsTA	NP_001353464.1:n.1019+49_1019+50delinsTA
NM_001366536.2:c.929+49_929+50delinsTA	NP_001353465.1:n.929+49_929+50delinsTA
NR_159362.2:n.1136+49_1136+50delinsTA
NM_144596.4:c.1049+49_1049+50delinsTA MANE Select	NP_653197.2:n.1049+49_1049+50delinsTA