Canonical Allele Identifier: CA2249872422

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028850_16028851delinsTC , CM000679.2:g.16028850_16028851delinsTC	GRCh38
NC_000017.10:g.15932164_15932165delinsTC , CM000679.1:g.15932164_15932165delinsTC	GRCh37
NC_000017.9:g.15872889_15872890delinsTC	NCBI36
NG_029806.1:g.34471_34472delinsTC
NG_047111.1:g.192896_192897delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1328_*1329delinsTC MANE Select	ENSP00000261647.5:n.*1328_*1329delinsTC
ENST00000261647.9:c.*1328_*1329delinsTC	ENSP00000261647.5:n.*1328_*1329delinsTC
ENST00000470649.1:c.247+2148_247+2149delinsTC	ENSP00000465627.1:n.247+2148_247+2149delinsTC
NM_001271420.1:c.*1328_*1329delinsTC	NP_001258349.1:n.*1328_*1329delinsTC
NM_017775.3:c.*1328_*1329delinsTC	NP_060245.3:n.*1328_*1329delinsTC
XM_017024801.2:c.994+2148_994+2149delinsTC	XP_016880290.2:n.994+2148_994+2149delinsTC
XM_017024802.2:c.994+2148_994+2149delinsTC	XP_016880291.2:n.994+2148_994+2149delinsTC
NM_017775.4:c.*1328_*1329delinsTC MANE Select	NP_060245.3:n.*1328_*1329delinsTC
NM_001271420.2:c.*1328_*1329delinsTC	NP_001258349.1:n.*1328_*1329delinsTC