Canonical Allele Identifier: CA705388799

Gene: TTC6

Linked Data

• dbSNP Id: rs1453135489
• gnomAD v3: 14-37608010-T-C
• gnomAD v4: 14-37608010-T-C
• MyVariant Identifiers: chr14:g.38077215T>C (hg19) ; chr14:g.37608010T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.37608010T>C , CM000676.2:g.37608010T>C	GRCh38
NC_000014.8:g.38077215T>C , CM000676.1:g.38077215T>C	GRCh37
NC_000014.7:g.37146966T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000553443.6:c.-16+1268T>C MANE Select	ENSP00000451131.1:n.-16+1268T>C
ENST00000556845.1:c.-155+1268T>C	ENSP00000450572.1:n.-155+1268T>C
NM_001310135.1:c.33+1268T>C	NP_001297064.1:n.33+1268T>C
XM_011537432.1:c.33+1268T>C	XP_011535734.1:n.33+1268T>C
XR_943762.1:n.890+1268T>C
XM_011537432.2:c.33+1268T>C	XP_011535734.1:n.33+1268T>C
XM_017021254.1:c.33+1268T>C	XP_016876743.1:n.33+1268T>C
XM_017021255.1:c.33+1268T>C	XP_016876744.1:n.33+1268T>C
XM_017021257.1:c.33+1268T>C	XP_016876746.1:n.33+1268T>C
XM_024449560.1:c.33+1268T>C	XP_024305328.1:n.33+1268T>C
XR_001750287.1:n.890+1268T>C
XR_943762.2:n.890+1268T>C
NM_001310135.2:c.33+1268T>C	NP_001297064.1:n.33+1268T>C
NM_001310135.3:c.33+1268T>C	NP_001297064.1:n.33+1268T>C
NM_001310135.5:c.-16+1268T>C MANE Select	NP_001297064.2:n.-16+1268T>C