Canonical Allele Identifier: CA2249870044

Gene: TTC19

Linked Data

• dbSNP Id: rs1714814424

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027614del , CM000679.2:g.16027614del	GRCh38
NC_000017.10:g.15930928del , CM000679.1:g.15930928del	GRCh37
NC_000017.9:g.15871653del	NCBI36
NG_029806.1:g.33235del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*92del MANE Select	ENSP00000261647.5:n.*92del
ENST00000261647.9:c.*92del	ENSP00000261647.5:n.*92del
ENST00000465567.1:n.1629del
ENST00000470649.1:c.247+912del	ENSP00000465627.1:n.247+912del
ENST00000475723.5:c.1419del
ENST00000481107.1:n.1903del
NM_001271420.1:c.*92del	NP_001258349.1:n.*92del
NM_017775.3:c.*92del	NP_060245.3:n.*92del
XM_017024801.2:c.994+912del	XP_016880290.2:n.994+912del
XM_017024802.2:c.994+912del	XP_016880291.2:n.994+912del
NM_017775.4:c.*92del MANE Select	NP_060245.3:n.*92del
NM_001271420.2:c.*92del	NP_001258349.1:n.*92del