Canonical Allele Identifier: CA464168700

Gene: TEK

Linked Data

• gnomAD v4: 9-27173313-C-G
• MyVariant Identifiers: chr9:g.27173311C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173313C>G , CM000671.2:g.27173313C>G	GRCh38
NC_000009.11:g.27173311C>G , CM000671.1:g.27173311C>G	GRCh37
NC_000009.10:g.27163311C>G	NCBI36
NG_011828.1:g.69165C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.852C>G MANE Select	ENSP00000369375.4:p.Pro284=
ENST00000380036.8:c.852C>G	ENSP00000369375.4:p.Pro284=
ENST00000406359.8:c.852C>G	ENSP00000383977.4:p.Pro284=
ENST00000519080.1:c.411C>G	ENSP00000428337.1:p.Pro137=
ENST00000519097.5:c.540C>G	ENSP00000430686.1:p.Pro180=
ENST00000615002.4:c.852C>G	ENSP00000480251.1:p.Pro284=
NM_000459.4:c.852C>G	NP_000450.2:p.Pro284=
NM_001290077.1:c.852C>G	NP_001277006.1:p.Pro284=
NM_001290078.1:c.540C>G	NP_001277007.1:p.Pro180=
XM_005251561.1:c.852C>G	XP_005251618.1:p.Pro284=
XM_005251563.1:c.852C>G	XP_005251620.1:p.Pro284=
XM_005251561.2:c.852C>G	XP_005251618.1:p.Pro284=
XM_005251563.2:c.852C>G	XP_005251620.1:p.Pro284=
NM_000459.5:c.852C>G MANE Select	NP_000450.3:p.Pro284=
NM_001375475.1:c.852C>G	NP_001362404.1:p.Pro284=
NM_001375476.1:c.852C>G	NP_001362405.1:p.Pro284=