Canonical Allele Identifier: CA1842031096
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27183480A= , CM000671.2:g.27183480A= GRCh38
NC_000009.11:g.27183478A= , CM000671.1:g.27183478A= GRCh37
NC_000009.10:g.27173478A= NCBI36
NG_011828.1:g.79332A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.1052A= MANE Select ENSP00000369375.4:p.Lys351=
ENST00000380036.8:c.1052A= ENSP00000369375.4:p.Lys351=
ENST00000406359.8:c.923A= ENSP00000383977.4:p.Lys308=
ENST00000519080.1:c.482A= ENSP00000428337.1:p.Lys161=
ENST00000519097.5:c.611A= ENSP00000430686.1:p.Lys204=
ENST00000615002.4:c.923A= ENSP00000480251.1:p.Lys308=
NM_000459.4:c.1052A= NP_000450.2:p.Lys351=
NM_001290077.1:c.923A= NP_001277006.1:p.Lys308=
NM_001290078.1:c.611A= NP_001277007.1:p.Lys204=
XM_005251561.1:c.1052A= XP_005251618.1:p.Lys351=
XM_005251563.1:c.923A= XP_005251620.1:p.Lys308=
XM_005251561.2:c.1052A= XP_005251618.1:p.Lys351=
XM_005251563.2:c.923A= XP_005251620.1:p.Lys308=
NM_000459.5:c.1052A= MANE Select NP_000450.3:p.Lys351=
NM_001375475.1:c.1052A= NP_001362404.1:p.Lys351=
NM_001375476.1:c.923A= NP_001362405.1:p.Lys308=