Canonical Allele Identifier: CA2249870746

Gene: TTC19

Linked Data

• dbSNP Id: rs1971644981

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028177del , CM000679.2:g.16028177del	GRCh38
NC_000017.10:g.15931491del , CM000679.1:g.15931491del	GRCh37
NC_000017.9:g.15872216del	NCBI36
NG_029806.1:g.33798del
NG_047111.1:g.193574del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*655del MANE Select	ENSP00000261647.5:n.*655del
ENST00000261647.9:c.*655del	ENSP00000261647.5:n.*655del
ENST00000465567.1:n.2192del
ENST00000470649.1:c.247+1475del	ENSP00000465627.1:n.247+1475del
ENST00000475723.5:c.1982del
ENST00000481107.1:n.2466del
NM_001271420.1:c.*655del	NP_001258349.1:n.*655del
NM_017775.3:c.*655del	NP_060245.3:n.*655del
XM_017024801.2:c.994+1475del	XP_016880290.2:n.994+1475del
XM_017024802.2:c.994+1475del	XP_016880291.2:n.994+1475del
NM_017775.4:c.*655del MANE Select	NP_060245.3:n.*655del
NM_001271420.2:c.*655del	NP_001258349.1:n.*655del