Canonical Allele Identifier: CA2249871728

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028740G= , CM000679.2:g.16028740G=	GRCh38
NC_000017.10:g.15932054G= , CM000679.1:g.15932054G=	GRCh37
NC_000017.9:g.15872779G=	NCBI36
NG_029806.1:g.34361G=
NG_047111.1:g.193007C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1218G= MANE Select	ENSP00000261647.5:n.*1218G=
ENST00000261647.9:c.*1218G=	ENSP00000261647.5:n.*1218G=
ENST00000465567.1:n.2755G=
ENST00000470649.1:c.247+2038G=	ENSP00000465627.1:n.247+2038G=
ENST00000475723.5:c.2545G=
ENST00000481107.1:n.3029G=
NM_001271420.1:c.*1218G=	NP_001258349.1:n.*1218G=
NM_017775.3:c.*1218G=	NP_060245.3:n.*1218G=
XM_017024801.2:c.994+2038G=	XP_016880290.2:n.994+2038G=
XM_017024802.2:c.994+2038G=	XP_016880291.2:n.994+2038G=
NM_017775.4:c.*1218G= MANE Select	NP_060245.3:n.*1218G=
NM_001271420.2:c.*1218G=	NP_001258349.1:n.*1218G=