Canonical Allele Identifier: CA2129956216
Gene: TTC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.37642610_37642612delinsTTA , CM000676.2:g.37642610_37642612delinsTTA GRCh38
NC_000014.8:g.38111815_38111817delinsTTA , CM000676.1:g.38111815_38111817delinsTTA GRCh37
NC_000014.7:g.37181566_37181568delinsTTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000553443.6:c.939+19607_939+19609delinsTTA MANE Select ENSP00000451131.1:n.939+19607_939+19609delinsTTA
ENST00000533625.5:c.939+19607_939+19609delinsTTA ENSP00000451566.1:n.939+19607_939+19609delinsTTA
ENST00000553443.5:c.939+19607_939+19609delinsTTA ENSP00000451131.1:n.939+19607_939+19609delinsTTA
NM_001310135.1:c.987+19607_987+19609delinsTTA NP_001297064.1:n.987+19607_987+19609delinsTTA
XM_011537432.1:c.987+19607_987+19609delinsTTA XP_011535734.1:n.987+19607_987+19609delinsTTA
XR_943762.1:n.1844+19607_1844+19609delinsTTA
XM_011537432.2:c.987+19607_987+19609delinsTTA XP_011535734.1:n.987+19607_987+19609delinsTTA
XM_017021254.1:c.987+19607_987+19609delinsTTA XP_016876743.1:n.987+19607_987+19609delinsTTA
XM_017021255.1:c.987+19607_987+19609delinsTTA XP_016876744.1:n.987+19607_987+19609delinsTTA
XM_017021257.1:c.987+19607_987+19609delinsTTA XP_016876746.1:n.987+19607_987+19609delinsTTA
XM_024449560.1:c.987+19607_987+19609delinsTTA XP_024305328.1:n.987+19607_987+19609delinsTTA
XR_001750287.1:n.1844+19607_1844+19609delinsTTA
XR_943762.2:n.1844+19607_1844+19609delinsTTA
NM_001310135.2:c.987+19607_987+19609delinsTTA NP_001297064.1:n.987+19607_987+19609delinsTTA
NM_001310135.3:c.987+19607_987+19609delinsTTA NP_001297064.1:n.987+19607_987+19609delinsTTA
NM_001310135.5:c.939+19607_939+19609delinsTTA MANE Select NP_001297064.2:n.939+19607_939+19609delinsTTA