Canonical Allele Identifier: CA2636262391

Gene: TTC19

Linked Data

• gnomAD v4: 17-16027570-G-GCTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027572_16027575dup , CM000679.2:g.16027572_16027575dup	GRCh38
NC_000017.10:g.15930886_15930889dup , CM000679.1:g.15930886_15930889dup	GRCh37
NC_000017.9:g.15871611_15871614dup	NCBI36
NG_029806.1:g.33193_33196dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*50_*53dup MANE Select	ENSP00000261647.5:n.*50_*53dup
ENST00000261647.9:c.*50_*53dup	ENSP00000261647.5:n.*50_*53dup
ENST00000465567.1:n.1587_1590dup
ENST00000470649.1:c.247+870_247+873dup	ENSP00000465627.1:n.247+870_247+873dup
ENST00000475723.5:c.1377_1380dup
ENST00000481107.1:n.1861_1864dup
NM_001271420.1:c.*50_*53dup	NP_001258349.1:n.*50_*53dup
NM_017775.3:c.*50_*53dup	NP_060245.3:n.*50_*53dup
XM_017024801.2:c.994+870_994+873dup	XP_016880290.2:n.994+870_994+873dup
XM_017024802.2:c.994+870_994+873dup	XP_016880291.2:n.994+870_994+873dup
NM_017775.4:c.*50_*53dup MANE Select	NP_060245.3:n.*50_*53dup
NM_001271420.2:c.*50_*53dup	NP_001258349.1:n.*50_*53dup