Canonical Allele Identifier: CA2249870051

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027621T= , CM000679.2:g.16027621T=	GRCh38
NC_000017.10:g.15930935T= , CM000679.1:g.15930935T=	GRCh37
NC_000017.9:g.15871660T=	NCBI36
NG_029806.1:g.33242T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*99T= MANE Select	ENSP00000261647.5:n.*99T=
ENST00000261647.9:c.*99T=	ENSP00000261647.5:n.*99T=
ENST00000465567.1:n.1636T=
ENST00000470649.1:c.247+919T=	ENSP00000465627.1:n.247+919T=
ENST00000475723.5:c.1426T=
ENST00000481107.1:n.1910T=
NM_001271420.1:c.*99T=	NP_001258349.1:n.*99T=
NM_017775.3:c.*99T=	NP_060245.3:n.*99T=
XM_017024801.2:c.994+919T=	XP_016880290.2:n.994+919T=
XM_017024802.2:c.994+919T=	XP_016880291.2:n.994+919T=
NM_017775.4:c.*99T= MANE Select	NP_060245.3:n.*99T=
NM_001271420.2:c.*99T=	NP_001258349.1:n.*99T=