Canonical Allele Identifier: CA2249870088

Gene: TTC19

Linked Data

• dbSNP Id: rs1971620165

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027664del , CM000679.2:g.16027664del	GRCh38
NC_000017.10:g.15930978del , CM000679.1:g.15930978del	GRCh37
NC_000017.9:g.15871703del	NCBI36
NG_029806.1:g.33285del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*142del MANE Select	ENSP00000261647.5:n.*142del
ENST00000261647.9:c.*142del	ENSP00000261647.5:n.*142del
ENST00000465567.1:n.1679del
ENST00000470649.1:c.247+962del	ENSP00000465627.1:n.247+962del
ENST00000475723.5:c.1469del
ENST00000481107.1:n.1953del
NM_001271420.1:c.*142del	NP_001258349.1:n.*142del
NM_017775.3:c.*142del	NP_060245.3:n.*142del
XM_017024801.2:c.994+962del	XP_016880290.2:n.994+962del
XM_017024802.2:c.994+962del	XP_016880291.2:n.994+962del
NM_017775.4:c.*142del MANE Select	NP_060245.3:n.*142del
NM_001271420.2:c.*142del	NP_001258349.1:n.*142del