Canonical Allele Identifier: CA259476577
Gene: TTC6 HGNC NCBI

Linked Data

dbSNP Id: rs553807943

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.37607983A>C , CM000676.2:g.37607983A>C GRCh38
NC_000014.8:g.38077188A>C , CM000676.1:g.38077188A>C GRCh37
NC_000014.7:g.37146939A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000553443.6:c.-16+1241A>C MANE Select ENSP00000451131.1:n.-16+1241A>C
ENST00000556845.1:c.-155+1241A>C ENSP00000450572.1:n.-155+1241A>C
NM_001310135.1:c.33+1241A>C NP_001297064.1:n.33+1241A>C
XM_011537432.1:c.33+1241A>C XP_011535734.1:n.33+1241A>C
XR_943762.1:n.890+1241A>C
XM_011537432.2:c.33+1241A>C XP_011535734.1:n.33+1241A>C
XM_017021254.1:c.33+1241A>C XP_016876743.1:n.33+1241A>C
XM_017021255.1:c.33+1241A>C XP_016876744.1:n.33+1241A>C
XM_017021257.1:c.33+1241A>C XP_016876746.1:n.33+1241A>C
XM_024449560.1:c.33+1241A>C XP_024305328.1:n.33+1241A>C
XR_001750287.1:n.890+1241A>C
XR_943762.2:n.890+1241A>C
NM_001310135.2:c.33+1241A>C NP_001297064.1:n.33+1241A>C
NM_001310135.3:c.33+1241A>C NP_001297064.1:n.33+1241A>C
NM_001310135.5:c.-16+1241A>C MANE Select NP_001297064.2:n.-16+1241A>C