Canonical Allele Identifier: CA2249870780

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028197_16028198delinsAC , CM000679.2:g.16028197_16028198delinsAC	GRCh38
NC_000017.10:g.15931511_15931512delinsAC , CM000679.1:g.15931511_15931512delinsAC	GRCh37
NC_000017.9:g.15872236_15872237delinsAC	NCBI36
NG_029806.1:g.33818_33819delinsAC
NG_047111.1:g.193549_193550delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*675_*676delinsAC MANE Select	ENSP00000261647.5:n.*675_*676delinsAC
ENST00000261647.9:c.*675_*676delinsAC	ENSP00000261647.5:n.*675_*676delinsAC
ENST00000465567.1:n.2212_2213delinsAC
ENST00000470649.1:c.247+1495_247+1496delinsAC	ENSP00000465627.1:n.247+1495_247+1496delinsAC
ENST00000475723.5:c.2002_2003delinsAC
ENST00000481107.1:n.2486_2487delinsAC
NM_001271420.1:c.*675_*676delinsAC	NP_001258349.1:n.*675_*676delinsAC
NM_017775.3:c.*675_*676delinsAC	NP_060245.3:n.*675_*676delinsAC
XM_017024801.2:c.994+1495_994+1496delinsAC	XP_016880290.2:n.994+1495_994+1496delinsAC
XM_017024802.2:c.994+1495_994+1496delinsAC	XP_016880291.2:n.994+1495_994+1496delinsAC
NM_017775.4:c.*675_*676delinsAC MANE Select	NP_060245.3:n.*675_*676delinsAC
NM_001271420.2:c.*675_*676delinsAC	NP_001258349.1:n.*675_*676delinsAC