Canonical Allele Identifier: CA2729488880

Gene: TTC6

Linked Data

• dbSNP Id: rs2139237954

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.37607866C>T , CM000676.2:g.37607866C>T	GRCh38
NC_000014.8:g.38077071C>T , CM000676.1:g.38077071C>T	GRCh37
NC_000014.7:g.37146822C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000553443.6:c.-16+1124C>T MANE Select	ENSP00000451131.1:n.-16+1124C>T
ENST00000556845.1:c.-155+1124C>T	ENSP00000450572.1:n.-155+1124C>T
NM_001310135.1:c.33+1124C>T	NP_001297064.1:n.33+1124C>T
XM_011537432.1:c.33+1124C>T	XP_011535734.1:n.33+1124C>T
XR_943762.1:n.890+1124C>T
XM_011537432.2:c.33+1124C>T	XP_011535734.1:n.33+1124C>T
XM_017021254.1:c.33+1124C>T	XP_016876743.1:n.33+1124C>T
XM_017021255.1:c.33+1124C>T	XP_016876744.1:n.33+1124C>T
XM_017021257.1:c.33+1124C>T	XP_016876746.1:n.33+1124C>T
XM_024449560.1:c.33+1124C>T	XP_024305328.1:n.33+1124C>T
XR_001750287.1:n.890+1124C>T
XR_943762.2:n.890+1124C>T
NM_001310135.2:c.33+1124C>T	NP_001297064.1:n.33+1124C>T
NM_001310135.3:c.33+1124C>T	NP_001297064.1:n.33+1124C>T
NM_001310135.5:c.-16+1124C>T MANE Select	NP_001297064.2:n.-16+1124C>T