Canonical Allele Identifier: CA2249871089

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028423_16028425delinsCTT , CM000679.2:g.16028423_16028425delinsCTT	GRCh38
NC_000017.10:g.15931737_15931739delinsCTT , CM000679.1:g.15931737_15931739delinsCTT	GRCh37
NC_000017.9:g.15872462_15872464delinsCTT	NCBI36
NG_029806.1:g.34044_34046delinsCTT
NG_047111.1:g.193322_193324delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*901_*903delinsCTT MANE Select	ENSP00000261647.5:n.*901_*903delinsCTT
ENST00000261647.9:c.*901_*903delinsCTT	ENSP00000261647.5:n.*901_*903delinsCTT
ENST00000465567.1:n.2438_2440delinsCTT
ENST00000470649.1:c.247+1721_247+1723delinsCTT	ENSP00000465627.1:n.247+1721_247+1723delinsCTT
ENST00000475723.5:c.2228_2230delinsCTT
ENST00000481107.1:n.2712_2714delinsCTT
NM_001271420.1:c.*901_*903delinsCTT	NP_001258349.1:n.*901_*903delinsCTT
NM_017775.3:c.*901_*903delinsCTT	NP_060245.3:n.*901_*903delinsCTT
XM_017024801.2:c.994+1721_994+1723delinsCTT	XP_016880290.2:n.994+1721_994+1723delinsCTT
XM_017024802.2:c.994+1721_994+1723delinsCTT	XP_016880291.2:n.994+1721_994+1723delinsCTT
NM_017775.4:c.*901_*903delinsCTT MANE Select	NP_060245.3:n.*901_*903delinsCTT
NM_001271420.2:c.*901_*903delinsCTT	NP_001258349.1:n.*901_*903delinsCTT