Canonical Allele Identifier: CA1842031089
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27183465A= , CM000671.2:g.27183465A= GRCh38
NC_000009.11:g.27183463A= , CM000671.1:g.27183463A= GRCh37
NC_000009.10:g.27173463A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.1037A= MANE Select ENSP00000369375.4:p.Gln346=
ENST00000380036.8:c.1037A= ENSP00000369375.4:p.Gln346=
ENST00000406359.8:c.908A= ENSP00000383977.4:p.Gln303=
ENST00000519080.1:c.467A= ENSP00000428337.1:p.Gln156=
ENST00000519097.5:c.596A= ENSP00000430686.1:p.Gln199=
ENST00000615002.4:c.908A= ENSP00000480251.1:p.Gln303=
XM_005251561.1:c.1037A= XP_005251618.1:p.Gln346=
XM_005251563.1:c.908A= XP_005251620.1:p.Gln303=
XM_005251561.2:c.1037A= XP_005251618.1:p.Gln346=
XM_005251563.2:c.908A= XP_005251620.1:p.Gln303=
NM_000459.5:c.1037A= MANE Select NP_000450.3:p.Gln346=
NM_001375475.1:c.1037A= NP_001362404.1:p.Gln346=
NM_001375476.1:c.908A= NP_001362405.1:p.Gln303=