Canonical Allele Identifier: CA1842021625

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173244C= , CM000671.2:g.27173244C=	GRCh38
NC_000009.11:g.27173242C= , CM000671.1:g.27173242C=	GRCh37
NC_000009.10:g.27163242C=	NCBI36
NG_011828.1:g.69096C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380036.10:c.783C= MANE Select	ENSP00000369375.4:p.Gly261=
ENST00000380036.8:c.783C=	ENSP00000369375.4:p.Gly261=
ENST00000406359.8:c.783C=	ENSP00000383977.4:p.Gly261=
ENST00000519080.1:c.342C=	ENSP00000428337.1:p.Gly114=
ENST00000519097.5:c.471C=	ENSP00000430686.1:p.Gly157=
ENST00000615002.4:c.783C=	ENSP00000480251.1:p.Gly261=
NM_000459.4:c.783C=	NP_000450.2:p.Gly261=
NM_001290077.1:c.783C=	NP_001277006.1:p.Gly261=
NM_001290078.1:c.471C=	NP_001277007.1:p.Gly157=
XM_005251561.1:c.783C=	XP_005251618.1:p.Gly261=
XM_005251563.1:c.783C=	XP_005251620.1:p.Gly261=
XM_005251561.2:c.783C=	XP_005251618.1:p.Gly261=
XM_005251563.2:c.783C=	XP_005251620.1:p.Gly261=
NM_000459.5:c.783C= MANE Select	NP_000450.3:p.Gly261=
NM_001375475.1:c.783C=	NP_001362404.1:p.Gly261=
NM_001375476.1:c.783C=	NP_001362405.1:p.Gly261=