Canonical Allele Identifier: CA2249870785

Gene: TTC19

Linked Data

• dbSNP Id: rs1971646799

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028198del , CM000679.2:g.16028198del	GRCh38
NC_000017.10:g.15931512del , CM000679.1:g.15931512del	GRCh37
NC_000017.9:g.15872237del	NCBI36
NG_029806.1:g.33819del
NG_047111.1:g.193549del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*676del MANE Select	ENSP00000261647.5:n.*676del
ENST00000261647.9:c.*676del	ENSP00000261647.5:n.*676del
ENST00000465567.1:n.2213del
ENST00000470649.1:c.247+1496del	ENSP00000465627.1:n.247+1496del
ENST00000475723.5:c.2003del
ENST00000481107.1:n.2487del
NM_001271420.1:c.*676del	NP_001258349.1:n.*676del
NM_017775.3:c.*676del	NP_060245.3:n.*676del
XM_017024801.2:c.994+1496del	XP_016880290.2:n.994+1496del
XM_017024802.2:c.994+1496del	XP_016880291.2:n.994+1496del
NM_017775.4:c.*676del MANE Select	NP_060245.3:n.*676del
NM_001271420.2:c.*676del	NP_001258349.1:n.*676del