Canonical Allele Identifier: CA2129935004

Gene: TTC6

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.37597370A= , CM000676.2:g.37597370A=	GRCh38
NC_000014.8:g.38066575A= , CM000676.1:g.38066575A=	GRCh37
NC_000014.7:g.37136326A=	NCBI36
NG_033028.1:g.2751T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001310135.5:c.-96+1362A= MANE Select	NP_001297064.2:n.-96+1362A=
ENST00000553443.6:c.-96+1362A= MANE Select	ENSP00000451131.1:n.-96+1362A=
NM_001310135.1:c.-48+1362A=	NP_001297064.1:n.-48+1362A=
NM_001310135.2:c.-48+1362A=	NP_001297064.1:n.-48+1362A=
NM_001310135.3:c.-48+1362A=	NP_001297064.1:n.-48+1362A=
ENST00000556845.1:c.-235+1362A=	ENSP00000450572.1:n.-235+1362A=
XM_011537432.1:c.-48+1362A=	XP_011535734.1:n.-48+1362A=
XM_011537432.2:c.-48+1362A=	XP_011535734.1:n.-48+1362A=
XM_017021254.1:c.-48+1362A=	XP_016876743.1:n.-48+1362A=
XM_017021255.1:c.-48+1362A=	XP_016876744.1:n.-48+1362A=
XM_017021257.1:c.-48+1362A=	XP_016876746.1:n.-48+1362A=
XM_024449560.1:c.-308+3816A=	XP_024305328.1:n.-308+3816A=
XR_001750287.1:n.810+1362A=
XR_943762.1:n.810+1362A=
XR_943762.2:n.810+1362A=