Canonical Allele Identifier: CA1842008668

Gene: TEK

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27212764G= , CM000671.2:g.27212764G=	GRCh38
NC_000009.11:g.27212762G= , CM000671.1:g.27212762G=	GRCh37
NC_000009.10:g.27202762G=	NCBI36
NG_011828.1:g.108616G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000459.5:c.2744G= MANE Select	NP_000450.3:p.Arg915=
ENST00000380036.10:c.2744G= MANE Select	ENSP00000369375.4:p.Arg915=
NM_000459.4:c.2744G=	NP_000450.2:p.Arg915=
NM_001290077.1:c.2615G=	NP_001277006.1:p.Arg872=
NM_001290078.1:c.2300G=	NP_001277007.1:p.Arg767=
NM_001375475.1:c.2741G=	NP_001362404.1:p.Arg914=
NM_001375476.1:c.2612G=	NP_001362405.1:p.Arg871=
ENST00000380036.8:c.2744G=	ENSP00000369375.4:p.Arg915=
ENST00000406359.8:c.2615G=	ENSP00000383977.4:p.Arg872=
ENST00000519097.5:c.2300G=	ENSP00000430686.1:p.Arg767=
ENST00000615002.4:c.*1245G=	ENSP00000480251.1:n.*1245G=
XM_005251561.1:c.2741G=	XP_005251618.1:p.Arg914=
XM_005251561.2:c.2741G=	XP_005251618.1:p.Arg914=
XM_005251563.1:c.2612G=	XP_005251620.1:p.Arg871=
XM_005251563.2:c.2612G=	XP_005251620.1:p.Arg871=