Canonical Allele Identifier: CA2129956203

Gene: TTC6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.37642581_37642583delinsCTT , CM000676.2:g.37642581_37642583delinsCTT	GRCh38
NC_000014.8:g.38111786_38111788delinsCTT , CM000676.1:g.38111786_38111788delinsCTT	GRCh37
NC_000014.7:g.37181537_37181539delinsCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553443.6:c.939+19578_939+19580delinsCTT MANE Select	ENSP00000451131.1:n.939+19578_939+19580delinsCTT
ENST00000533625.5:c.939+19578_939+19580delinsCTT	ENSP00000451566.1:n.939+19578_939+19580delinsCTT
ENST00000553443.5:c.939+19578_939+19580delinsCTT	ENSP00000451131.1:n.939+19578_939+19580delinsCTT
NM_001310135.1:c.987+19578_987+19580delinsCTT	NP_001297064.1:n.987+19578_987+19580delinsCTT
XM_011537432.1:c.987+19578_987+19580delinsCTT	XP_011535734.1:n.987+19578_987+19580delinsCTT
XR_943762.1:n.1844+19578_1844+19580delinsCTT
XM_011537432.2:c.987+19578_987+19580delinsCTT	XP_011535734.1:n.987+19578_987+19580delinsCTT
XM_017021254.1:c.987+19578_987+19580delinsCTT	XP_016876743.1:n.987+19578_987+19580delinsCTT
XM_017021255.1:c.987+19578_987+19580delinsCTT	XP_016876744.1:n.987+19578_987+19580delinsCTT
XM_017021257.1:c.987+19578_987+19580delinsCTT	XP_016876746.1:n.987+19578_987+19580delinsCTT
XM_024449560.1:c.987+19578_987+19580delinsCTT	XP_024305328.1:n.987+19578_987+19580delinsCTT
XR_001750287.1:n.1844+19578_1844+19580delinsCTT
XR_943762.2:n.1844+19578_1844+19580delinsCTT
NM_001310135.2:c.987+19578_987+19580delinsCTT	NP_001297064.1:n.987+19578_987+19580delinsCTT
NM_001310135.3:c.987+19578_987+19580delinsCTT	NP_001297064.1:n.987+19578_987+19580delinsCTT
NM_001310135.5:c.939+19578_939+19580delinsCTT MANE Select	NP_001297064.2:n.939+19578_939+19580delinsCTT