Canonical Allele Identifier: CA705410278

Gene: TTC6

Linked Data

• dbSNP Id: rs1444849451
• MyVariant Identifiers: chr14:g.38111774T>C (hg19) ; chr14:g.37642569T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.37642569T>C , CM000676.2:g.37642569T>C	GRCh38
NC_000014.8:g.38111774T>C , CM000676.1:g.38111774T>C	GRCh37
NC_000014.7:g.37181525T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000553443.6:c.939+19566T>C MANE Select	ENSP00000451131.1:n.939+19566T>C
ENST00000533625.5:c.939+19566T>C	ENSP00000451566.1:n.939+19566T>C
ENST00000553443.5:c.939+19566T>C	ENSP00000451131.1:n.939+19566T>C
NM_001310135.1:c.987+19566T>C	NP_001297064.1:n.987+19566T>C
XM_011537432.1:c.987+19566T>C	XP_011535734.1:n.987+19566T>C
XR_943762.1:n.1844+19566T>C
XM_011537432.2:c.987+19566T>C	XP_011535734.1:n.987+19566T>C
XM_017021254.1:c.987+19566T>C	XP_016876743.1:n.987+19566T>C
XM_017021255.1:c.987+19566T>C	XP_016876744.1:n.987+19566T>C
XM_017021257.1:c.987+19566T>C	XP_016876746.1:n.987+19566T>C
XM_024449560.1:c.987+19566T>C	XP_024305328.1:n.987+19566T>C
XR_001750287.1:n.1844+19566T>C
XR_943762.2:n.1844+19566T>C
NM_001310135.2:c.987+19566T>C	NP_001297064.1:n.987+19566T>C
NM_001310135.3:c.987+19566T>C	NP_001297064.1:n.987+19566T>C
NM_001310135.5:c.939+19566T>C MANE Select	NP_001297064.2:n.939+19566T>C