Canonical Allele Identifier: CA2249870043

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027613_16027614delinsCT , CM000679.2:g.16027613_16027614delinsCT	GRCh38
NC_000017.10:g.15930927_15930928delinsCT , CM000679.1:g.15930927_15930928delinsCT	GRCh37
NC_000017.9:g.15871652_15871653delinsCT	NCBI36
NG_029806.1:g.33234_33235delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*91_*92delinsCT MANE Select	ENSP00000261647.5:n.*91_*92delinsCT
ENST00000261647.9:c.*91_*92delinsCT	ENSP00000261647.5:n.*91_*92delinsCT
ENST00000465567.1:n.1628_1629delinsCT
ENST00000470649.1:c.247+911_247+912delinsCT	ENSP00000465627.1:n.247+911_247+912delinsCT
ENST00000475723.5:c.1418_1419delinsCT
ENST00000481107.1:n.1902_1903delinsCT
NM_001271420.1:c.*91_*92delinsCT	NP_001258349.1:n.*91_*92delinsCT
NM_017775.3:c.*91_*92delinsCT	NP_060245.3:n.*91_*92delinsCT
XM_017024801.2:c.994+911_994+912delinsCT	XP_016880290.2:n.994+911_994+912delinsCT
XM_017024802.2:c.994+911_994+912delinsCT	XP_016880291.2:n.994+911_994+912delinsCT
NM_017775.4:c.*91_*92delinsCT MANE Select	NP_060245.3:n.*91_*92delinsCT
NM_001271420.2:c.*91_*92delinsCT	NP_001258349.1:n.*91_*92delinsCT