Canonical Allele Identifier: CA2636262694

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028059-TACCAGCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028060_16028066del , CM000679.2:g.16028060_16028066del	GRCh38
NC_000017.10:g.15931374_15931380del , CM000679.1:g.15931374_15931380del	GRCh37
NC_000017.9:g.15872099_15872105del	NCBI36
NG_029806.1:g.33681_33687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*538_*544del MANE Select	ENSP00000261647.5:n.*538_*544del
ENST00000261647.9:c.*538_*544del	ENSP00000261647.5:n.*538_*544del
ENST00000465567.1:n.2075_2081del
ENST00000470649.1:c.247+1358_247+1364del	ENSP00000465627.1:n.247+1358_247+1364del
ENST00000475723.5:c.1865_1871del
ENST00000481107.1:n.2349_2355del
NM_001271420.1:c.*538_*544del	NP_001258349.1:n.*538_*544del
NM_017775.3:c.*538_*544del	NP_060245.3:n.*538_*544del
XM_017024801.2:c.994+1358_994+1364del	XP_016880290.2:n.994+1358_994+1364del
XM_017024802.2:c.994+1358_994+1364del	XP_016880291.2:n.994+1358_994+1364del
NM_017775.4:c.*538_*544del MANE Select	NP_060245.3:n.*538_*544del
NM_001271420.2:c.*538_*544del	NP_001258349.1:n.*538_*544del