Canonical Allele Identifier: CA398379647
Gene: TTC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16027520T>G , CM000679.2:g.16027520T>G GRCh38
NC_000017.10:g.15930834T>G , CM000679.1:g.15930834T>G GRCh37
NC_000017.9:g.15871559T>G NCBI36
NG_029806.1:g.33141T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.1141T>G MANE Select ENSP00000261647.5:p.Ter381Glu
ENST00000261647.9:c.1141T>G ENSP00000261647.5:p.Ter381Glu
ENST00000465567.1:n.1535T>G
ENST00000470649.1:c.247+818T>G ENSP00000465627.1:n.247+818T>G
ENST00000475723.5:c.1325T>G
ENST00000481107.1:n.1809T>G
ENST00000497842.6:n.1345T>G
NM_001271420.1:c.820T>G NP_001258349.1:p.Ter274Glu
NM_017775.3:c.1141T>G NP_060245.3:p.Ter381Glu
XM_017024801.2:c.994+818T>G XP_016880290.2:n.994+818T>G
XM_017024802.2:c.994+818T>G XP_016880291.2:n.994+818T>G
NM_017775.4:c.1141T>G MANE Select NP_060245.3:p.Ter381Glu
NM_001271420.2:c.820T>G NP_001258349.1:p.Ter274Glu