Canonical Allele Identifier: CA364644554
Community Standard Title: NM_003318.5(TTK):c.1051A>G (p.Thr351Ala)
Gene: TTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.80014529A>G , CM000668.2:g.80014529A>G GRCh38
NC_000006.11:g.80724246A>G , CM000668.1:g.80724246A>G GRCh37
NC_000006.10:g.80780965A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_003318.5:c.1051A>G MANE Select NP_003309.2:p.Thr351Ala
ENST00000369798.7:c.1051A>G MANE Select ENSP00000358813.2:p.Thr351Ala
NM_001166691.1:c.1051A>G NP_001160163.1:p.Thr351Ala
NM_001166691.2:c.1051A>G NP_001160163.1:p.Thr351Ala
NM_003318.4:c.1051A>G NP_003309.2:p.Thr351Ala
ENST00000230510.7:c.1051A>G ENSP00000230510.3:p.Thr351Ala
ENST00000369798.6:c.1051A>G ENSP00000358813.2:p.Thr351Ala
ENST00000509894.5:c.1051A>G ENSP00000422936.1:p.Thr351Ala
ENST00000515751.1:n.175A>G
XM_011536099.1:c.1051A>G XP_011534401.1:p.Thr351Ala
XM_011536099.3:c.1051A>G XP_011534401.1:p.Thr351Ala
XM_011536100.1:c.1051A>G XP_011534402.1:p.Thr351Ala
XM_011536100.3:c.1051A>G XP_011534402.1:p.Thr351Ala
XM_017011242.2:c.886A>G XP_016866731.1:p.Thr296Ala