Canonical Allele Identifier: CA2783322723

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173514_27173515insG , CM000671.2:g.27173514_27173515insG	GRCh38
NC_000009.11:g.27173512_27173513insG , CM000671.1:g.27173512_27173513insG	GRCh37
NC_000009.10:g.27163512_27163513insG	NCBI36
NG_011828.1:g.69366_69367insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.901+152_901+153insG MANE Select	ENSP00000369375.4:n.901+152_901+153insG
ENST00000380036.8:c.901+152_901+153insG	ENSP00000369375.4:n.901+152_901+153insG
ENST00000406359.8:c.901+152_901+153insG	ENSP00000383977.4:n.901+152_901+153insG
ENST00000519080.1:c.460+152_460+153insG	ENSP00000428337.1:n.460+152_460+153insG
ENST00000519097.5:c.589+152_589+153insG	ENSP00000430686.1:n.589+152_589+153insG
ENST00000615002.4:c.901+152_901+153insG	ENSP00000480251.1:n.901+152_901+153insG
NM_000459.4:c.901+152_901+153insG	NP_000450.2:n.901+152_901+153insG
NM_001290077.1:c.901+152_901+153insG	NP_001277006.1:n.901+152_901+153insG
NM_001290078.1:c.589+152_589+153insG	NP_001277007.1:n.589+152_589+153insG
XM_005251561.1:c.901+152_901+153insG	XP_005251618.1:n.901+152_901+153insG
XM_005251563.1:c.901+152_901+153insG	XP_005251620.1:n.901+152_901+153insG
XM_005251561.2:c.901+152_901+153insG	XP_005251618.1:n.901+152_901+153insG
XM_005251563.2:c.901+152_901+153insG	XP_005251620.1:n.901+152_901+153insG
NM_000459.5:c.901+152_901+153insG MANE Select	NP_000450.3:n.901+152_901+153insG
NM_001375475.1:c.901+152_901+153insG	NP_001362404.1:n.901+152_901+153insG
NM_001375476.1:c.901+152_901+153insG	NP_001362405.1:n.901+152_901+153insG