Canonical Allele Identifier: CA1842021812

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173357A= , CM000671.2:g.27173357A=	GRCh38
NC_000009.11:g.27173355A= , CM000671.1:g.27173355A=	GRCh37
NC_000009.10:g.27163355A=	NCBI36
NG_011828.1:g.69209A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.896A= MANE Select	ENSP00000369375.4:p.Asn299=
ENST00000380036.8:c.896A=	ENSP00000369375.4:p.Asn299=
ENST00000406359.8:c.896A=	ENSP00000383977.4:p.Asn299=
ENST00000519080.1:c.455A=	ENSP00000428337.1:p.Asn152=
ENST00000519097.5:c.584A=	ENSP00000430686.1:p.Asn195=
ENST00000615002.4:c.896A=	ENSP00000480251.1:p.Asn299=
NM_000459.4:c.896A=	NP_000450.2:p.Asn299=
NM_001290077.1:c.896A=	NP_001277006.1:p.Asn299=
NM_001290078.1:c.584A=	NP_001277007.1:p.Asn195=
XM_005251561.1:c.896A=	XP_005251618.1:p.Asn299=
XM_005251563.1:c.896A=	XP_005251620.1:p.Asn299=
XM_005251561.2:c.896A=	XP_005251618.1:p.Asn299=
XM_005251563.2:c.896A=	XP_005251620.1:p.Asn299=
NM_000459.5:c.896A= MANE Select	NP_000450.3:p.Asn299=
NM_001375475.1:c.896A=	NP_001362404.1:p.Asn299=
NM_001375476.1:c.896A=	NP_001362405.1:p.Asn299=