Canonical Allele Identifier: CA464168693

Gene: TEK

Linked Data

• gnomAD v4: 9-27173307-T-A
• MyVariant Identifiers: chr9:g.27173305T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.27173307T>A , CM000671.2:g.27173307T>A	GRCh38
NC_000009.11:g.27173305T>A , CM000671.1:g.27173305T>A	GRCh37
NC_000009.10:g.27163305T>A	NCBI36
NG_011828.1:g.69159T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380036.10:c.846T>A MANE Select	ENSP00000369375.4:p.Pro282=
ENST00000380036.8:c.846T>A	ENSP00000369375.4:p.Pro282=
ENST00000406359.8:c.846T>A	ENSP00000383977.4:p.Pro282=
ENST00000519080.1:c.405T>A	ENSP00000428337.1:p.Pro135=
ENST00000519097.5:c.534T>A	ENSP00000430686.1:p.Pro178=
ENST00000615002.4:c.846T>A	ENSP00000480251.1:p.Pro282=
NM_000459.4:c.846T>A	NP_000450.2:p.Pro282=
NM_001290077.1:c.846T>A	NP_001277006.1:p.Pro282=
NM_001290078.1:c.534T>A	NP_001277007.1:p.Pro178=
XM_005251561.1:c.846T>A	XP_005251618.1:p.Pro282=
XM_005251563.1:c.846T>A	XP_005251620.1:p.Pro282=
XM_005251561.2:c.846T>A	XP_005251618.1:p.Pro282=
XM_005251563.2:c.846T>A	XP_005251620.1:p.Pro282=
NM_000459.5:c.846T>A MANE Select	NP_000450.3:p.Pro282=
NM_001375475.1:c.846T>A	NP_001362404.1:p.Pro282=
NM_001375476.1:c.846T>A	NP_001362405.1:p.Pro282=