Canonical Allele Identifier: CA2249869961

Gene: TTC19

Linked Data

• dbSNP Id: rs1971609700
• gnomAD v4: 17-16027560-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027561_16027562del , CM000679.2:g.16027561_16027562del	GRCh38
NC_000017.10:g.15930875_15930876del , CM000679.1:g.15930875_15930876del	GRCh37
NC_000017.9:g.15871600_15871601del	NCBI36
NG_029806.1:g.33182_33183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*39_*40del MANE Select	ENSP00000261647.5:n.*39_*40del
ENST00000261647.9:c.*39_*40del	ENSP00000261647.5:n.*39_*40del
ENST00000465567.1:n.1576_1577del
ENST00000470649.1:c.247+859_247+860del	ENSP00000465627.1:n.247+859_247+860del
ENST00000475723.5:c.1366_1367del
ENST00000481107.1:n.1850_1851del
NM_001271420.1:c.*39_*40del	NP_001258349.1:n.*39_*40del
NM_017775.3:c.*39_*40del	NP_060245.3:n.*39_*40del
XM_017024801.2:c.994+859_994+860del	XP_016880290.2:n.994+859_994+860del
XM_017024802.2:c.994+859_994+860del	XP_016880291.2:n.994+859_994+860del
NM_017775.4:c.*39_*40del MANE Select	NP_060245.3:n.*39_*40del
NM_001271420.2:c.*39_*40del	NP_001258349.1:n.*39_*40del