Canonical Allele Identifier: CA2636262439

Gene: TTC19

Linked Data

• gnomAD v4: 17-16027676-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027678del , CM000679.2:g.16027678del	GRCh38
NC_000017.10:g.15930992del , CM000679.1:g.15930992del	GRCh37
NC_000017.9:g.15871717del	NCBI36
NG_029806.1:g.33299del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*156del MANE Select	ENSP00000261647.5:n.*156del
ENST00000261647.9:c.*156del	ENSP00000261647.5:n.*156del
ENST00000465567.1:n.1693del
ENST00000470649.1:c.247+976del	ENSP00000465627.1:n.247+976del
ENST00000475723.5:c.1483del
ENST00000481107.1:n.1967del
NM_001271420.1:c.*156del	NP_001258349.1:n.*156del
NM_017775.3:c.*156del	NP_060245.3:n.*156del
XM_017024801.2:c.994+976del	XP_016880290.2:n.994+976del
XM_017024802.2:c.994+976del	XP_016880291.2:n.994+976del
NM_017775.4:c.*156del MANE Select	NP_060245.3:n.*156del
NM_001271420.2:c.*156del	NP_001258349.1:n.*156del