Canonical Allele Identifier: CA2802515226

Gene: TTC8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.88833466_88833594del , CM000676.2:g.88833466_88833594del	GRCh38
NC_000014.8:g.89299810_89299938del , CM000676.1:g.89299810_89299938del	GRCh37
NC_000014.7:g.88369563_88369691del	NCBI36
NG_008126.1:g.13833_13961del
NG_008126.2:g.14314_14442del

Transcript Alleles

HGVS	Amino-acid change
ENST00000380656.7:c.115-227_115-99del MANE Select	ENSP00000370031.2:n.115-227_115-99del
ENST00000338104.10:c.115-5986_115-5858del	ENSP00000337653.6:n.115-5986_115-5858del
ENST00000345383.9:c.115-227_115-99del	ENSP00000339486.6:n.115-227_115-99del
ENST00000346301.8:c.115-5986_115-5858del	ENSP00000298324.6:n.115-5986_115-5858del
ENST00000354441.10:c.114+8645_114+8773del	ENSP00000346427.6:n.114+8645_114+8773del
ENST00000358622.9:c.-448-5986_-448-5858del	ENSP00000351439.5:n.-448-5986_-448-5858del
ENST00000380656.6:c.115-227_115-99del	ENSP00000370031.2:n.115-227_115-99del
ENST00000536576.5:c.115-5986_115-5858del	ENSP00000445067.2:n.115-5986_115-5858del
ENST00000553718.1:c.*149-450_*149-322del	ENSP00000450905.1:n.*149-450_*149-322del
ENST00000554686.5:c.84-5986_84-5858del
ENST00000555057.5:c.115-5986_115-5858del	ENSP00000450951.1:n.115-5986_115-5858del
ENST00000556077.5:c.115-3442_115-3314del	ENSP00000451034.1:n.115-3442_115-3314del
ENST00000556567.5:n.172-5986_172-5858del
ENST00000556651.5:c.115-5986_115-5858del	ENSP00000450993.1:n.115-5986_115-5858del
ENST00000614125.4:c.115-5986_115-5858del	ENSP00000482306.1:n.115-5986_115-5858del
ENST00000622513.4:c.115-5986_115-5858del	ENSP00000482721.1:n.115-5986_115-5858del
NM_001288781.1:c.115-5986_115-5858del	NP_001275710.1:n.115-5986_115-5858del
NM_001288782.1:c.-448-5986_-448-5858del	NP_001275711.1:n.-448-5986_-448-5858del
NM_001288783.1:c.-543-5986_-543-5858del	NP_001275712.1:n.-543-5986_-543-5858del
NM_144596.3:c.115-227_115-99del	NP_653197.2:n.115-227_115-99del
NM_198309.3:c.115-5986_115-5858del	NP_938051.1:n.115-5986_115-5858del
NM_198310.3:c.115-5986_115-5858del	NP_938052.1:n.115-5986_115-5858del
XM_006720035.1:c.115-5986_115-5858del	XP_006720098.1:n.115-5986_115-5858del
XM_006720037.2:c.115-5986_115-5858del	XP_006720100.1:n.115-5986_115-5858del
XM_011536432.1:c.115-5986_115-5858del	XP_011534734.1:n.115-5986_115-5858del
XM_011536433.1:c.115-5986_115-5858del	XP_011534735.1:n.115-5986_115-5858del
XM_011536434.1:c.115-5986_115-5858del	XP_011534736.1:n.115-5986_115-5858del
NM_001366535.1:c.115-5986_115-5858del	NP_001353464.1:n.115-5986_115-5858del
NM_001366536.1:c.115-5986_115-5858del	NP_001353465.1:n.115-5986_115-5858del
NR_159362.1:n.172-5986_172-5858del
XM_011536433.2:c.115-5986_115-5858del	XP_011534735.1:n.115-5986_115-5858del
XM_011536434.2:c.115-5986_115-5858del	XP_011534736.1:n.115-5986_115-5858del
NM_001366535.2:c.115-5986_115-5858del	NP_001353464.1:n.115-5986_115-5858del
NM_001366536.2:c.115-5986_115-5858del	NP_001353465.1:n.115-5986_115-5858del
NR_159362.2:n.172-5986_172-5858del
NM_144596.4:c.115-227_115-99del MANE Select	NP_653197.2:n.115-227_115-99del