Canonical Allele Identifier: CA2249869968

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027565G= , CM000679.2:g.16027565G=	GRCh38
NC_000017.10:g.15930879G= , CM000679.1:g.15930879G=	GRCh37
NC_000017.9:g.15871604G=	NCBI36
NG_029806.1:g.33186G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*43G= MANE Select	ENSP00000261647.5:n.*43G=
ENST00000261647.9:c.*43G=	ENSP00000261647.5:n.*43G=
ENST00000465567.1:n.1580G=
ENST00000470649.1:c.247+863G=	ENSP00000465627.1:n.247+863G=
ENST00000475723.5:c.1370G=
ENST00000481107.1:n.1854G=
NM_001271420.1:c.*43G=	NP_001258349.1:n.*43G=
NM_017775.3:c.*43G=	NP_060245.3:n.*43G=
XM_017024801.2:c.994+863G=	XP_016880290.2:n.994+863G=
XM_017024802.2:c.994+863G=	XP_016880291.2:n.994+863G=
NM_017775.4:c.*43G= MANE Select	NP_060245.3:n.*43G=
NM_001271420.2:c.*43G=	NP_001258349.1:n.*43G=