Canonical Allele Identifier: CA1842030937
Gene: TEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27183099_27183101delinsAAG , CM000671.2:g.27183099_27183101delinsAAG GRCh38
NC_000009.11:g.27183097_27183099delinsAAG , CM000671.1:g.27183097_27183099delinsAAG GRCh37
NC_000009.10:g.27173097_27173099delinsAAG NCBI36
NG_011828.1:g.78951_78953delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.1031-360_1031-358delinsAAG MANE Select ENSP00000369375.4:n.1031-360_1031-358delinsAAG
ENST00000380036.8:c.1031-360_1031-358delinsAAG ENSP00000369375.4:n.1031-360_1031-358delinsAAG
ENST00000406359.8:c.902-360_902-358delinsAAG ENSP00000383977.4:n.902-360_902-358delinsAAG
ENST00000519080.1:c.461-360_461-358delinsAAG ENSP00000428337.1:n.461-360_461-358delinsAAG
ENST00000519097.5:c.590-360_590-358delinsAAG ENSP00000430686.1:n.590-360_590-358delinsAAG
ENST00000615002.4:c.902-360_902-358delinsAAG ENSP00000480251.1:n.902-360_902-358delinsAAG
NM_000459.4:c.1031-360_1031-358delinsAAG NP_000450.2:n.1031-360_1031-358delinsAAG
NM_001290077.1:c.902-360_902-358delinsAAG NP_001277006.1:n.902-360_902-358delinsAAG
NM_001290078.1:c.590-360_590-358delinsAAG NP_001277007.1:n.590-360_590-358delinsAAG
XM_005251561.1:c.1031-360_1031-358delinsAAG XP_005251618.1:n.1031-360_1031-358delinsAAG
XM_005251563.1:c.902-360_902-358delinsAAG XP_005251620.1:n.902-360_902-358delinsAAG
XM_005251561.2:c.1031-360_1031-358delinsAAG XP_005251618.1:n.1031-360_1031-358delinsAAG
XM_005251563.2:c.902-360_902-358delinsAAG XP_005251620.1:n.902-360_902-358delinsAAG
NM_000459.5:c.1031-360_1031-358delinsAAG MANE Select NP_000450.3:n.1031-360_1031-358delinsAAG
NM_001375475.1:c.1031-360_1031-358delinsAAG NP_001362404.1:n.1031-360_1031-358delinsAAG
NM_001375476.1:c.902-360_902-358delinsAAG NP_001362405.1:n.902-360_902-358delinsAAG