Canonical Allele Identifier: CA2249814947

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999853T= , CM000679.2:g.15999853T=	GRCh38
NC_000017.10:g.15903167T= , CM000679.1:g.15903167T=	GRCh37
NC_000017.9:g.15843892T=	NCBI36
NG_029806.1:g.5474T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.5T= MANE Select	ENSP00000261647.5:p.Phe2=
ENST00000261647.9:c.5T=	ENSP00000261647.5:p.Phe2=
ENST00000466729.5:c.70T=
ENST00000470399.1:c.20T=	ENSP00000465082.1:p.Phe7=
ENST00000475723.5:c.52T=
ENST00000497842.6:n.30T=
ENST00000583704.1:n.30T=
NM_001271420.1:c.-454T=	NP_001258349.1:n.-454T=
NM_017775.3:c.5T=	NP_060245.3:p.Phe2=
XM_011523950.1:c.5T=	XP_011522252.1:p.Phe2=
XM_017024801.2:c.5T=	XP_016880290.2:p.Phe2=
XM_017024802.2:c.5T=	XP_016880291.2:p.Phe2=
XM_024450814.1:c.5T=	XP_024306582.1:p.Phe2=
NM_017775.4:c.5T= MANE Select	NP_060245.3:p.Phe2=
NM_001271420.2:c.-454T=	NP_001258349.1:n.-454T=