Canonical Allele Identifier: CA398388469
Gene: TTC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16006497A>T , CM000679.2:g.16006497A>T GRCh38
NC_000017.10:g.15909811A>T , CM000679.1:g.15909811A>T GRCh37
NC_000017.9:g.15850536A>T NCBI36
NG_029806.1:g.12118A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.605A>T MANE Select ENSP00000261647.5:p.Tyr202Phe
ENST00000261647.9:c.605A>T ENSP00000261647.5:p.Tyr202Phe
ENST00000475723.5:c.789A>T
ENST00000497842.6:n.715A>T
NM_001271420.1:c.284A>T NP_001258349.1:p.Tyr95Phe
NM_017775.3:c.605A>T NP_060245.3:p.Tyr202Phe
XM_011523950.1:c.605A>T XP_011522252.1:p.Tyr202Phe
XR_934261.1:n.1791+666T>A
XM_017024801.2:c.605A>T XP_016880290.2:p.Tyr202Phe
XM_017024802.2:c.605A>T XP_016880291.2:p.Tyr202Phe
XM_024450814.1:c.605A>T XP_024306582.1:p.Tyr202Phe
NM_017775.4:c.605A>T MANE Select NP_060245.3:p.Tyr202Phe
NM_001271420.2:c.284A>T NP_001258349.1:p.Tyr95Phe