Canonical Allele Identifier: CA2249870046

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027618_16027619delinsGT , CM000679.2:g.16027618_16027619delinsGT	GRCh38
NC_000017.10:g.15930932_15930933delinsGT , CM000679.1:g.15930932_15930933delinsGT	GRCh37
NC_000017.9:g.15871657_15871658delinsGT	NCBI36
NG_029806.1:g.33239_33240delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*96_*97delinsGT MANE Select	ENSP00000261647.5:n.*96_*97delinsGT
ENST00000261647.9:c.*96_*97delinsGT	ENSP00000261647.5:n.*96_*97delinsGT
ENST00000465567.1:n.1633_1634delinsGT
ENST00000470649.1:c.247+916_247+917delinsGT	ENSP00000465627.1:n.247+916_247+917delinsGT
ENST00000475723.5:c.1423_1424delinsGT
ENST00000481107.1:n.1907_1908delinsGT
NM_001271420.1:c.*96_*97delinsGT	NP_001258349.1:n.*96_*97delinsGT
NM_017775.3:c.*96_*97delinsGT	NP_060245.3:n.*96_*97delinsGT
XM_017024801.2:c.994+916_994+917delinsGT	XP_016880290.2:n.994+916_994+917delinsGT
XM_017024802.2:c.994+916_994+917delinsGT	XP_016880291.2:n.994+916_994+917delinsGT
NM_017775.4:c.*96_*97delinsGT MANE Select	NP_060245.3:n.*96_*97delinsGT
NM_001271420.2:c.*96_*97delinsGT	NP_001258349.1:n.*96_*97delinsGT