Canonical Allele Identifier: CA1842008650
Community Standard Title: NM_000459.5(TEK):c.2690A= (p.Tyr897=)
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27212710A= , CM000671.2:g.27212710A= GRCh38
NC_000009.11:g.27212708A= , CM000671.1:g.27212708A= GRCh37
NC_000009.10:g.27202708A= NCBI36
NG_011828.1:g.108562A=

Transcript Alleles

HGVS Amino-acid Change
NM_000459.5:c.2690A= MANE Select NP_000450.3:p.Tyr897=
ENST00000380036.10:c.2690A= MANE Select ENSP00000369375.4:p.Tyr897=
NM_000459.4:c.2690A= NP_000450.2:p.Tyr897=
NM_001290077.1:c.2561A= NP_001277006.1:p.Tyr854=
NM_001290078.1:c.2246A= NP_001277007.1:p.Tyr749=
NM_001375475.1:c.2687A= NP_001362404.1:p.Tyr896=
NM_001375476.1:c.2558A= NP_001362405.1:p.Tyr853=
ENST00000380036.8:c.2690A= ENSP00000369375.4:p.Tyr897=
ENST00000406359.8:c.2561A= ENSP00000383977.4:p.Tyr854=
ENST00000519097.5:c.2246A= ENSP00000430686.1:p.Tyr749=
ENST00000615002.4:c.*1191A= ENSP00000480251.1:n.*1191A=
XM_005251561.1:c.2687A= XP_005251618.1:p.Tyr896=
XM_005251561.2:c.2687A= XP_005251618.1:p.Tyr896=
XM_005251563.1:c.2558A= XP_005251620.1:p.Tyr853=
XM_005251563.2:c.2558A= XP_005251620.1:p.Tyr853=