Canonical Allele Identifier: CA2249822057

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16006503T= , CM000679.2:g.16006503T=	GRCh38
NC_000017.10:g.15909817T= , CM000679.1:g.15909817T=	GRCh37
NC_000017.9:g.15850542T=	NCBI36
NG_029806.1:g.12124T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.611T= MANE Select	ENSP00000261647.5:p.Phe204=
ENST00000261647.9:c.611T=	ENSP00000261647.5:p.Phe204=
ENST00000475723.5:c.795T=
ENST00000497842.6:n.721T=
NM_001271420.1:c.290T=	NP_001258349.1:p.Phe97=
NM_017775.3:c.611T=	NP_060245.3:p.Phe204=
XM_011523950.1:c.611T=	XP_011522252.1:p.Phe204=
XR_934261.1:n.1791+660A=
XM_017024801.2:c.611T=	XP_016880290.2:p.Phe204=
XM_017024802.2:c.611T=	XP_016880291.2:p.Phe204=
XM_024450814.1:c.611T=	XP_024306582.1:p.Phe204=
NM_017775.4:c.611T= MANE Select	NP_060245.3:p.Phe204=
NM_001271420.2:c.290T=	NP_001258349.1:p.Phe97=