Canonical Allele Identifier: CA2129940154

Gene: TTC6

Linked Data

• dbSNP Id: rs2095627705

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.37607692_37607693insC , CM000676.2:g.37607692_37607693insC	GRCh38
NC_000014.8:g.38076897_38076898insC , CM000676.1:g.38076897_38076898insC	GRCh37
NC_000014.7:g.37146648_37146649insC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000553443.6:c.-16+950_-16+951insC MANE Select	ENSP00000451131.1:n.-16+950_-16+951insC
ENST00000556845.1:c.-155+950_-155+951insC	ENSP00000450572.1:n.-155+950_-155+951insC
NM_001310135.1:c.33+950_33+951insC	NP_001297064.1:n.33+950_33+951insC
XM_011537432.1:c.33+950_33+951insC	XP_011535734.1:n.33+950_33+951insC
XR_943762.1:n.890+950_890+951insC
XM_011537432.2:c.33+950_33+951insC	XP_011535734.1:n.33+950_33+951insC
XM_017021254.1:c.33+950_33+951insC	XP_016876743.1:n.33+950_33+951insC
XM_017021255.1:c.33+950_33+951insC	XP_016876744.1:n.33+950_33+951insC
XM_017021257.1:c.33+950_33+951insC	XP_016876746.1:n.33+950_33+951insC
XM_024449560.1:c.33+950_33+951insC	XP_024305328.1:n.33+950_33+951insC
XR_001750287.1:n.890+950_890+951insC
XR_943762.2:n.890+950_890+951insC
NM_001310135.2:c.33+950_33+951insC	NP_001297064.1:n.33+950_33+951insC
NM_001310135.3:c.33+950_33+951insC	NP_001297064.1:n.33+950_33+951insC
NM_001310135.5:c.-16+950_-16+951insC MANE Select	NP_001297064.2:n.-16+950_-16+951insC