Canonical Allele Identifier: CA2249871153

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028470_16028474delinsATTCT , CM000679.2:g.16028470_16028474delinsATTCT	GRCh38
NC_000017.10:g.15931784_15931788delinsATTCT , CM000679.1:g.15931784_15931788delinsATTCT	GRCh37
NC_000017.9:g.15872509_15872513delinsATTCT	NCBI36
NG_029806.1:g.34091_34095delinsATTCT
NG_047111.1:g.193273_193277delinsAGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*948_*952delinsATTCT MANE Select	ENSP00000261647.5:n.*948_*952delinsATTCT
ENST00000261647.9:c.*948_*952delinsATTCT	ENSP00000261647.5:n.*948_*952delinsATTCT
ENST00000465567.1:n.2485_2489delinsATTCT
ENST00000470649.1:c.247+1768_247+1772delinsATTCT	ENSP00000465627.1:n.247+1768_247+1772delinsATTCT
ENST00000475723.5:c.2275_2279delinsATTCT
ENST00000481107.1:n.2759_2763delinsATTCT
NM_001271420.1:c.*948_*952delinsATTCT	NP_001258349.1:n.*948_*952delinsATTCT
NM_017775.3:c.*948_*952delinsATTCT	NP_060245.3:n.*948_*952delinsATTCT
XM_017024801.2:c.994+1768_994+1772delinsATTCT	XP_016880290.2:n.994+1768_994+1772delinsATTCT
XM_017024802.2:c.994+1768_994+1772delinsATTCT	XP_016880291.2:n.994+1768_994+1772delinsATTCT
NM_017775.4:c.*948_*952delinsATTCT MANE Select	NP_060245.3:n.*948_*952delinsATTCT
NM_001271420.2:c.*948_*952delinsATTCT	NP_001258349.1:n.*948_*952delinsATTCT