Canonical Allele Identifier: CA1842008664
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27212753G= , CM000671.2:g.27212753G= GRCh38
NC_000009.11:g.27212751G= , CM000671.1:g.27212751G= GRCh37
NC_000009.10:g.27202751G= NCBI36
NG_011828.1:g.108605G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.2733G= MANE Select ENSP00000369375.4:p.Leu911=
ENST00000380036.8:c.2733G= ENSP00000369375.4:p.Leu911=
ENST00000406359.8:c.2604G= ENSP00000383977.4:p.Leu868=
ENST00000519097.5:c.2289G= ENSP00000430686.1:p.Leu763=
ENST00000615002.4:c.*1234G= ENSP00000480251.1:n.*1234G=
NM_000459.4:c.2733G= NP_000450.2:p.Leu911=
NM_001290077.1:c.2604G= NP_001277006.1:p.Leu868=
NM_001290078.1:c.2289G= NP_001277007.1:p.Leu763=
XM_005251561.1:c.2730G= XP_005251618.1:p.Leu910=
XM_005251563.1:c.2601G= XP_005251620.1:p.Leu867=
XM_005251561.2:c.2730G= XP_005251618.1:p.Leu910=
XM_005251563.2:c.2601G= XP_005251620.1:p.Leu867=
NM_000459.5:c.2733G= MANE Select NP_000450.3:p.Leu911=
NM_001375475.1:c.2730G= NP_001362404.1:p.Leu910=
NM_001375476.1:c.2601G= NP_001362405.1:p.Leu867=