Canonical Allele Identifier: CA16486592

Gene: TTC6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.37795751A>G , CM000676.2:g.37795751A>G	GRCh38
NC_000014.8:g.38264956A>G , CM000676.1:g.38264956A>G	GRCh37
NC_000014.7:g.37334707A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553443.6:c.3791+399A>G MANE Select	ENSP00000451131.1:n.3791+399A>G
ENST00000267368.11:c.-17+399A>G	ENSP00000267368.7:n.-17+399A>G
ENST00000382320.4:c.-68+399A>G	ENSP00000371757.4:n.-68+399A>G
ENST00000476979.5:c.-17+399A>G	ENSP00000417788.1:n.-17+399A>G
ENST00000478811.6:c.-17+399A>G	ENSP00000419204.2:n.-17+399A>G
ENST00000533625.5:c.*1062+56596A>G	ENSP00000451566.1:n.*1062+56596A>G
ENST00000553443.5:c.3791+399A>G	ENSP00000451131.1:n.3791+399A>G
NM_001310135.1:c.3839+399A>G	NP_001297064.1:n.3839+399A>G
XM_011537430.1:c.2396+399A>G	XP_011535732.1:n.2396+399A>G
XM_011537431.1:c.2078+399A>G	XP_011535733.1:n.2078+399A>G
XR_943762.1:n.4696+399A>G
XM_011537430.2:c.2396+399A>G	XP_011535732.1:n.2396+399A>G
XM_011537431.2:c.2078+399A>G	XP_011535733.1:n.2078+399A>G
XM_017021254.1:c.3839+399A>G	XP_016876743.1:n.3839+399A>G
XM_017021255.1:c.3839+399A>G	XP_016876744.1:n.3839+399A>G
XM_017021256.1:c.2840+399A>G	XP_016876745.1:n.2840+399A>G
XM_024449560.1:c.3839+399A>G	XP_024305328.1:n.3839+399A>G
XR_943762.2:n.4696+399A>G
NM_001310135.2:c.3839+399A>G	NP_001297064.1:n.3839+399A>G
NM_001368142.1:c.-17+399A>G	NP_001355071.1:n.-17+399A>G
NM_001310135.3:c.3839+399A>G	NP_001297064.1:n.3839+399A>G
NM_001368142.2:c.-17+399A>G	NP_001355071.1:n.-17+399A>G
NM_001310135.5:c.3791+399A>G MANE Select	NP_001297064.2:n.3791+399A>G