Canonical Allele Identifier: CA2636262388

Gene: TTC19

Linked Data

• gnomAD v4: 17-16027547-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027548del , CM000679.2:g.16027548del	GRCh38
NC_000017.10:g.15930862del , CM000679.1:g.15930862del	GRCh37
NC_000017.9:g.15871587del	NCBI36
NG_029806.1:g.33169del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*26del MANE Select	ENSP00000261647.5:n.*26del
ENST00000261647.9:c.*26del	ENSP00000261647.5:n.*26del
ENST00000465567.1:n.1563del
ENST00000470649.1:c.247+846del	ENSP00000465627.1:n.247+846del
ENST00000475723.5:c.1353del
ENST00000481107.1:n.1837del
NM_001271420.1:c.*26del	NP_001258349.1:n.*26del
NM_017775.3:c.*26del	NP_060245.3:n.*26del
XM_017024801.2:c.994+846del	XP_016880290.2:n.994+846del
XM_017024802.2:c.994+846del	XP_016880291.2:n.994+846del
NM_017775.4:c.*26del MANE Select	NP_060245.3:n.*26del
NM_001271420.2:c.*26del	NP_001258349.1:n.*26del