Canonical Allele Identifier: CA2249870025

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027599T= , CM000679.2:g.16027599T=	GRCh38
NC_000017.10:g.15930913T= , CM000679.1:g.15930913T=	GRCh37
NC_000017.9:g.15871638T=	NCBI36
NG_029806.1:g.33220T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*77T= MANE Select	ENSP00000261647.5:n.*77T=
ENST00000261647.9:c.*77T=	ENSP00000261647.5:n.*77T=
ENST00000465567.1:n.1614T=
ENST00000470649.1:c.247+897T=	ENSP00000465627.1:n.247+897T=
ENST00000475723.5:c.1404T=
ENST00000481107.1:n.1888T=
NM_001271420.1:c.*77T=	NP_001258349.1:n.*77T=
NM_017775.3:c.*77T=	NP_060245.3:n.*77T=
XM_017024801.2:c.994+897T=	XP_016880290.2:n.994+897T=
XM_017024802.2:c.994+897T=	XP_016880291.2:n.994+897T=
NM_017775.4:c.*77T= MANE Select	NP_060245.3:n.*77T=
NM_001271420.2:c.*77T=	NP_001258349.1:n.*77T=