Canonical Allele Identifier: CA398382625
Gene: TTC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16000002C>T , CM000679.2:g.16000002C>T GRCh38
NC_000017.10:g.15903316C>T , CM000679.1:g.15903316C>T GRCh37
NC_000017.9:g.15844041C>T NCBI36
NG_029806.1:g.5623C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.154C>T MANE Select ENSP00000261647.5:p.Arg52Trp
ENST00000261647.9:c.154C>T ENSP00000261647.5:p.Arg52Trp
ENST00000466729.5:c.219C>T
ENST00000470399.1:c.169C>T ENSP00000465082.1:p.Arg57Trp
ENST00000475723.5:c.201C>T
ENST00000497842.6:n.179C>T
ENST00000583704.1:n.179C>T
NM_001271420.1:c.-305C>T NP_001258349.1:n.-305C>T
NM_017775.3:c.154C>T NP_060245.3:p.Arg52Trp
XM_011523950.1:c.154C>T XP_011522252.1:p.Arg52Trp
XM_017024801.2:c.154C>T XP_016880290.2:p.Arg52Trp
XM_017024802.2:c.154C>T XP_016880291.2:p.Arg52Trp
XM_024450814.1:c.154C>T XP_024306582.1:p.Arg52Trp
NM_017775.4:c.154C>T MANE Select NP_060245.3:p.Arg52Trp
NM_001271420.2:c.-305C>T NP_001258349.1:n.-305C>T