Canonical Allele Identifier: CA373125843

Gene: TEK

Linked Data

• MyVariant Identifiers: chr9:g.27173330A>C (hg19) ; chr9:g.27173332A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173332A>C , CM000671.2:g.27173332A>C	GRCh38
NC_000009.11:g.27173330A>C , CM000671.1:g.27173330A>C	GRCh37
NC_000009.10:g.27163330A>C	NCBI36
NG_011828.1:g.69184A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.871A>C MANE Select	ENSP00000369375.4:p.Thr291Pro
ENST00000380036.8:c.871A>C	ENSP00000369375.4:p.Thr291Pro
ENST00000406359.8:c.871A>C	ENSP00000383977.4:p.Thr291Pro
ENST00000519080.1:c.430A>C	ENSP00000428337.1:p.Thr144Pro
ENST00000519097.5:c.559A>C	ENSP00000430686.1:p.Thr187Pro
ENST00000615002.4:c.871A>C	ENSP00000480251.1:p.Thr291Pro
NM_000459.4:c.871A>C	NP_000450.2:p.Thr291Pro
NM_001290077.1:c.871A>C	NP_001277006.1:p.Thr291Pro
NM_001290078.1:c.559A>C	NP_001277007.1:p.Thr187Pro
XM_005251561.1:c.871A>C	XP_005251618.1:p.Thr291Pro
XM_005251563.1:c.871A>C	XP_005251620.1:p.Thr291Pro
XM_005251561.2:c.871A>C	XP_005251618.1:p.Thr291Pro
XM_005251563.2:c.871A>C	XP_005251620.1:p.Thr291Pro
NM_000459.5:c.871A>C MANE Select	NP_000450.3:p.Thr291Pro
NM_001375475.1:c.871A>C	NP_001362404.1:p.Thr291Pro
NM_001375476.1:c.871A>C	NP_001362405.1:p.Thr291Pro