Canonical Allele Identifier: CA2129940237
Gene: TTC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.37607910A= , CM000676.2:g.37607910A= GRCh38
NC_000014.8:g.38077115A= , CM000676.1:g.38077115A= GRCh37
NC_000014.7:g.37146866A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000553443.6:c.-16+1168A= MANE Select ENSP00000451131.1:n.-16+1168A=
ENST00000556845.1:c.-155+1168A= ENSP00000450572.1:n.-155+1168A=
NM_001310135.1:c.33+1168A= NP_001297064.1:n.33+1168A=
XM_011537432.1:c.33+1168A= XP_011535734.1:n.33+1168A=
XR_943762.1:n.890+1168A=
XM_011537432.2:c.33+1168A= XP_011535734.1:n.33+1168A=
XM_017021254.1:c.33+1168A= XP_016876743.1:n.33+1168A=
XM_017021255.1:c.33+1168A= XP_016876744.1:n.33+1168A=
XM_017021257.1:c.33+1168A= XP_016876746.1:n.33+1168A=
XM_024449560.1:c.33+1168A= XP_024305328.1:n.33+1168A=
XR_001750287.1:n.890+1168A=
XR_943762.2:n.890+1168A=
NM_001310135.2:c.33+1168A= NP_001297064.1:n.33+1168A=
NM_001310135.3:c.33+1168A= NP_001297064.1:n.33+1168A=
NM_001310135.5:c.-16+1168A= MANE Select NP_001297064.2:n.-16+1168A=