Canonical Allele Identifier: CA5016062

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27180230C>T , CM000671.2:g.27180230C>T	GRCh38
NC_000009.11:g.27180228C>T , CM000671.1:g.27180228C>T	GRCh37
NC_000009.10:g.27170228C>T	NCBI36
NG_011828.1:g.76082C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.902-10C>T MANE Select	ENSP00000369375.4:n.902-10C>T
ENST00000380036.8:c.902-10C>T	ENSP00000369375.4:n.902-10C>T
ENST00000406359.8:c.902-3229C>T	ENSP00000383977.4:n.902-3229C>T
ENST00000519080.1:c.461-3229C>T	ENSP00000428337.1:n.461-3229C>T
ENST00000519097.5:c.590-3229C>T	ENSP00000430686.1:n.590-3229C>T
ENST00000615002.4:c.902-3229C>T	ENSP00000480251.1:n.902-3229C>T
NM_000459.4:c.902-10C>T	NP_000450.2:n.902-10C>T
NM_001290077.1:c.902-3229C>T	NP_001277006.1:n.902-3229C>T
NM_001290078.1:c.590-3229C>T	NP_001277007.1:n.590-3229C>T
XM_005251561.1:c.902-10C>T	XP_005251618.1:n.902-10C>T
XM_005251563.1:c.902-3229C>T	XP_005251620.1:n.902-3229C>T
XM_005251561.2:c.902-10C>T	XP_005251618.1:n.902-10C>T
XM_005251563.2:c.902-3229C>T	XP_005251620.1:n.902-3229C>T
NM_000459.5:c.902-10C>T MANE Select	NP_000450.3:n.902-10C>T
NM_001375475.1:c.902-10C>T	NP_001362404.1:n.902-10C>T
NM_001375476.1:c.902-3229C>T	NP_001362405.1:n.902-3229C>T