Canonical Allele Identifier: CA2129940250
Gene: TTC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.37607944_37607948delinsTCTTA , CM000676.2:g.37607944_37607948delinsTCTTA GRCh38
NC_000014.8:g.38077149_38077153delinsTCTTA , CM000676.1:g.38077149_38077153delinsTCTTA GRCh37
NC_000014.7:g.37146900_37146904delinsTCTTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000553443.6:c.-16+1202_-16+1206delinsTCTTA MANE Select ENSP00000451131.1:n.-16+1202_-16+1206deli...
ENST00000556845.1:c.-155+1202_-155+1206delinsTCTTA ENSP00000450572.1:n.-155+1202_-155+1206de...
NM_001310135.1:c.33+1202_33+1206delinsTCTTA NP_001297064.1:n.33+1202_33+1206delinsTCT...
XM_011537432.1:c.33+1202_33+1206delinsTCTTA XP_011535734.1:n.33+1202_33+1206delinsTCT...
XR_943762.1:n.890+1202_890+1206delinsTCTTA
XM_011537432.2:c.33+1202_33+1206delinsTCTTA XP_011535734.1:n.33+1202_33+1206delinsTCT...
XM_017021254.1:c.33+1202_33+1206delinsTCTTA XP_016876743.1:n.33+1202_33+1206delinsTCT...
XM_017021255.1:c.33+1202_33+1206delinsTCTTA XP_016876744.1:n.33+1202_33+1206delinsTCT...
XM_017021257.1:c.33+1202_33+1206delinsTCTTA XP_016876746.1:n.33+1202_33+1206delinsTCT...
XM_024449560.1:c.33+1202_33+1206delinsTCTTA XP_024305328.1:n.33+1202_33+1206delinsTCT...
XR_001750287.1:n.890+1202_890+1206delinsTCTTA
XR_943762.2:n.890+1202_890+1206delinsTCTTA
NM_001310135.2:c.33+1202_33+1206delinsTCTTA NP_001297064.1:n.33+1202_33+1206delinsTCT...
NM_001310135.3:c.33+1202_33+1206delinsTCTTA NP_001297064.1:n.33+1202_33+1206delinsTCT...
NM_001310135.5:c.-16+1202_-16+1206delinsTCTTA MANE Select NP_001297064.2:n.-16+1202_-16+1206delinsT...