Canonical Allele Identifier: CA2636259687
Gene: TTC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999901_15999916del , CM000679.2:g.15999901_15999916del GRCh38
NC_000017.10:g.15903215_15903230del , CM000679.1:g.15903215_15903230del GRCh37
NC_000017.9:g.15843940_15843955del NCBI36
NG_029806.1:g.5522_5537del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.53_68del MANE Select ENSP00000261647.5:p.Gly18AlafsTer?
ENST00000261647.9:c.53_68del ENSP00000261647.5:p.Gly18AlafsTer?
ENST00000466729.5:c.118_133del
ENST00000470399.1:c.68_83del ENSP00000465082.1:p.Gly23AlafsTer?
ENST00000475723.5:c.100_115del
ENST00000497842.6:n.78_93del
ENST00000583704.1:n.78_93del
NM_001271420.1:c.-406_-391del NP_001258349.1:n.-406_-391del
NM_017775.3:c.53_68del NP_060245.3:p.Gly18AlafsTer?
XM_011523950.1:c.53_68del XP_011522252.1:p.Gly18AlafsTer?
XM_017024801.2:c.53_68del XP_016880290.2:p.Gly18AlafsTer?
XM_017024802.2:c.53_68del XP_016880291.2:p.Gly18AlafsTer?
XM_024450814.1:c.53_68del XP_024306582.1:p.Gly18AlafsTer?
NM_017775.4:c.53_68del MANE Select NP_060245.3:p.Gly18AlafsTer?
NM_001271420.2:c.-406_-391del NP_001258349.1:n.-406_-391del