Canonical Allele Identifier: CA2129940248
Gene: TTC6 HGNC NCBI

Linked Data

dbSNP Id: rs2095628078

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.37607941T>A , CM000676.2:g.37607941T>A GRCh38
NC_000014.8:g.38077146T>A , CM000676.1:g.38077146T>A GRCh37
NC_000014.7:g.37146897T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000553443.6:c.-16+1199T>A MANE Select ENSP00000451131.1:n.-16+1199T>A
ENST00000556845.1:c.-155+1199T>A ENSP00000450572.1:n.-155+1199T>A
NM_001310135.1:c.33+1199T>A NP_001297064.1:n.33+1199T>A
XM_011537432.1:c.33+1199T>A XP_011535734.1:n.33+1199T>A
XR_943762.1:n.890+1199T>A
XM_011537432.2:c.33+1199T>A XP_011535734.1:n.33+1199T>A
XM_017021254.1:c.33+1199T>A XP_016876743.1:n.33+1199T>A
XM_017021255.1:c.33+1199T>A XP_016876744.1:n.33+1199T>A
XM_017021257.1:c.33+1199T>A XP_016876746.1:n.33+1199T>A
XM_024449560.1:c.33+1199T>A XP_024305328.1:n.33+1199T>A
XR_001750287.1:n.890+1199T>A
XR_943762.2:n.890+1199T>A
NM_001310135.2:c.33+1199T>A NP_001297064.1:n.33+1199T>A
NM_001310135.3:c.33+1199T>A NP_001297064.1:n.33+1199T>A
NM_001310135.5:c.-16+1199T>A MANE Select NP_001297064.2:n.-16+1199T>A