Canonical Allele Identifier: CA2636259689
Gene: TTC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999921_15999945del , CM000679.2:g.15999921_15999945del GRCh38
NC_000017.10:g.15903235_15903259del , CM000679.1:g.15903235_15903259del GRCh37
NC_000017.9:g.15843960_15843984del NCBI36
NG_029806.1:g.5542_5566del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.73_97del MANE Select ENSP00000261647.5:p.Ser25GlnfsTer?
ENST00000261647.9:c.73_97del ENSP00000261647.5:p.Ser25GlnfsTer?
ENST00000466729.5:c.138_162del
ENST00000470399.1:c.88_112del ENSP00000465082.1:p.Ser30GlnfsTer?
ENST00000475723.5:c.120_144del
ENST00000497842.6:n.98_122del
ENST00000583704.1:n.98_122del
NM_001271420.1:c.-386_-362del NP_001258349.1:n.-386_-362del
NM_017775.3:c.73_97del NP_060245.3:p.Ser25GlnfsTer?
XM_011523950.1:c.73_97del XP_011522252.1:p.Ser25GlnfsTer?
XM_017024801.2:c.73_97del XP_016880290.2:p.Ser25GlnfsTer?
XM_017024802.2:c.73_97del XP_016880291.2:p.Ser25GlnfsTer?
XM_024450814.1:c.73_97del XP_024306582.1:p.Ser25GlnfsTer?
NM_017775.4:c.73_97del MANE Select NP_060245.3:p.Ser25GlnfsTer?
NM_001271420.2:c.-386_-362del NP_001258349.1:n.-386_-362del