Canonical Allele Identifier: CA2591248436
Gene: TTC6 HGNC NCBI

Linked Data

dbSNP Id: rs2139238221

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.37607937C>T , CM000676.2:g.37607937C>T GRCh38
NC_000014.8:g.38077142C>T , CM000676.1:g.38077142C>T GRCh37
NC_000014.7:g.37146893C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000553443.6:c.-16+1195C>T MANE Select ENSP00000451131.1:n.-16+1195C>T
ENST00000556845.1:c.-155+1195C>T ENSP00000450572.1:n.-155+1195C>T
NM_001310135.1:c.33+1195C>T NP_001297064.1:n.33+1195C>T
XM_011537432.1:c.33+1195C>T XP_011535734.1:n.33+1195C>T
XR_943762.1:n.890+1195C>T
XM_011537432.2:c.33+1195C>T XP_011535734.1:n.33+1195C>T
XM_017021254.1:c.33+1195C>T XP_016876743.1:n.33+1195C>T
XM_017021255.1:c.33+1195C>T XP_016876744.1:n.33+1195C>T
XM_017021257.1:c.33+1195C>T XP_016876746.1:n.33+1195C>T
XM_024449560.1:c.33+1195C>T XP_024305328.1:n.33+1195C>T
XR_001750287.1:n.890+1195C>T
XR_943762.2:n.890+1195C>T
NM_001310135.2:c.33+1195C>T NP_001297064.1:n.33+1195C>T
NM_001310135.3:c.33+1195C>T NP_001297064.1:n.33+1195C>T
NM_001310135.5:c.-16+1195C>T MANE Select NP_001297064.2:n.-16+1195C>T