Canonical Allele Identifier: CA1842021703
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27173300G= , CM000671.2:g.27173300G= GRCh38
NC_000009.11:g.27173298G= , CM000671.1:g.27173298G= GRCh37
NC_000009.10:g.27163298G= NCBI36
NG_011828.1:g.69152G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.839G= MANE Select ENSP00000369375.4:p.Cys280=
ENST00000380036.8:c.839G= ENSP00000369375.4:p.Cys280=
ENST00000406359.8:c.839G= ENSP00000383977.4:p.Cys280=
ENST00000519080.1:c.398G= ENSP00000428337.1:p.Cys133=
ENST00000519097.5:c.527G= ENSP00000430686.1:p.Cys176=
ENST00000615002.4:c.839G= ENSP00000480251.1:p.Cys280=
NM_000459.4:c.839G= NP_000450.2:p.Cys280=
NM_001290077.1:c.839G= NP_001277006.1:p.Cys280=
NM_001290078.1:c.527G= NP_001277007.1:p.Cys176=
XM_005251561.1:c.839G= XP_005251618.1:p.Cys280=
XM_005251563.1:c.839G= XP_005251620.1:p.Cys280=
XM_005251561.2:c.839G= XP_005251618.1:p.Cys280=
XM_005251563.2:c.839G= XP_005251620.1:p.Cys280=
NM_000459.5:c.839G= MANE Select NP_000450.3:p.Cys280=
NM_001375475.1:c.839G= NP_001362404.1:p.Cys280=
NM_001375476.1:c.839G= NP_001362405.1:p.Cys280=