Canonical Allele Identifier: CA2249870061

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027629_16027630delinsTC , CM000679.2:g.16027629_16027630delinsTC	GRCh38
NC_000017.10:g.15930943_15930944delinsTC , CM000679.1:g.15930943_15930944delinsTC	GRCh37
NC_000017.9:g.15871668_15871669delinsTC	NCBI36
NG_029806.1:g.33250_33251delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*107_*108delinsTC MANE Select	ENSP00000261647.5:n.*107_*108delinsTC
ENST00000261647.9:c.*107_*108delinsTC	ENSP00000261647.5:n.*107_*108delinsTC
ENST00000465567.1:n.1644_1645delinsTC
ENST00000470649.1:c.247+927_247+928delinsTC	ENSP00000465627.1:n.247+927_247+928delinsTC
ENST00000475723.5:c.1434_1435delinsTC
ENST00000481107.1:n.1918_1919delinsTC
NM_001271420.1:c.*107_*108delinsTC	NP_001258349.1:n.*107_*108delinsTC
NM_017775.3:c.*107_*108delinsTC	NP_060245.3:n.*107_*108delinsTC
XM_017024801.2:c.994+927_994+928delinsTC	XP_016880290.2:n.994+927_994+928delinsTC
XM_017024802.2:c.994+927_994+928delinsTC	XP_016880291.2:n.994+927_994+928delinsTC
NM_017775.4:c.*107_*108delinsTC MANE Select	NP_060245.3:n.*107_*108delinsTC
NM_001271420.2:c.*107_*108delinsTC	NP_001258349.1:n.*107_*108delinsTC