Canonical Allele Identifier: CA2741521499

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028542del , CM000679.2:g.16028542del	GRCh38
NC_000017.10:g.15931856del , CM000679.1:g.15931856del	GRCh37
NC_000017.9:g.15872581del	NCBI36
NG_029806.1:g.34163del
NG_047111.1:g.193205del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1020del MANE Select	ENSP00000261647.5:n.*1020del
ENST00000261647.9:c.*1020del	ENSP00000261647.5:n.*1020del
ENST00000465567.1:n.2557del
ENST00000470649.1:c.247+1840del	ENSP00000465627.1:n.247+1840del
ENST00000475723.5:c.2347del
ENST00000481107.1:n.2831del
NM_001271420.1:c.*1020del	NP_001258349.1:n.*1020del
NM_017775.3:c.*1020del	NP_060245.3:n.*1020del
XM_017024801.2:c.994+1840del	XP_016880290.2:n.994+1840del
XM_017024802.2:c.994+1840del	XP_016880291.2:n.994+1840del
NM_017775.4:c.*1020del MANE Select	NP_060245.3:n.*1020del
NM_001271420.2:c.*1020del	NP_001258349.1:n.*1020del