Canonical Allele Identifier: CA2249871190

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028491A= , CM000679.2:g.16028491A=	GRCh38
NC_000017.10:g.15931805A= , CM000679.1:g.15931805A=	GRCh37
NC_000017.9:g.15872530A=	NCBI36
NG_029806.1:g.34112A=
NG_047111.1:g.193256T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*969A= MANE Select	ENSP00000261647.5:n.*969A=
ENST00000261647.9:c.*969A=	ENSP00000261647.5:n.*969A=
ENST00000465567.1:n.2506A=
ENST00000470649.1:c.247+1789A=	ENSP00000465627.1:n.247+1789A=
ENST00000475723.5:c.2296A=
ENST00000481107.1:n.2780A=
NM_001271420.1:c.*969A=	NP_001258349.1:n.*969A=
NM_017775.3:c.*969A=	NP_060245.3:n.*969A=
XM_017024801.2:c.994+1789A=	XP_016880290.2:n.994+1789A=
XM_017024802.2:c.994+1789A=	XP_016880291.2:n.994+1789A=
NM_017775.4:c.*969A= MANE Select	NP_060245.3:n.*969A=
NM_001271420.2:c.*969A=	NP_001258349.1:n.*969A=