Canonical Allele Identifier: CA2249870064

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027632G= , CM000679.2:g.16027632G=	GRCh38
NC_000017.10:g.15930946G= , CM000679.1:g.15930946G=	GRCh37
NC_000017.9:g.15871671G=	NCBI36
NG_029806.1:g.33253G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*110G= MANE Select	ENSP00000261647.5:n.*110G=
ENST00000261647.9:c.*110G=	ENSP00000261647.5:n.*110G=
ENST00000465567.1:n.1647G=
ENST00000470649.1:c.247+930G=	ENSP00000465627.1:n.247+930G=
ENST00000475723.5:c.1437G=
ENST00000481107.1:n.1921G=
NM_001271420.1:c.*110G=	NP_001258349.1:n.*110G=
NM_017775.3:c.*110G=	NP_060245.3:n.*110G=
XM_017024801.2:c.994+930G=	XP_016880290.2:n.994+930G=
XM_017024802.2:c.994+930G=	XP_016880291.2:n.994+930G=
NM_017775.4:c.*110G= MANE Select	NP_060245.3:n.*110G=
NM_001271420.2:c.*110G=	NP_001258349.1:n.*110G=