Canonical Allele Identifier: CA5016028
Gene: TEK HGNC NCBI

Linked Data

dbSNP Id: rs759617301
gnomAD v2: 9-27173290-T-C
gnomAD v3: 9-27173292-T-C
gnomAD v4: 9-27173292-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27173292T>C , CM000671.2:g.27173292T>C GRCh38
NC_000009.11:g.27173290T>C , CM000671.1:g.27173290T>C GRCh37
NC_000009.10:g.27163290T>C NCBI36
NG_011828.1:g.69144T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380036.10:c.831T>C MANE Select ENSP00000369375.4:p.Tyr277=
ENST00000380036.8:c.831T>C ENSP00000369375.4:p.Tyr277=
ENST00000406359.8:c.831T>C ENSP00000383977.4:p.Tyr277=
ENST00000519080.1:c.390T>C ENSP00000428337.1:p.Tyr130=
ENST00000519097.5:c.519T>C ENSP00000430686.1:p.Tyr173=
ENST00000615002.4:c.831T>C ENSP00000480251.1:p.Tyr277=
NM_000459.4:c.831T>C NP_000450.2:p.Tyr277=
NM_001290077.1:c.831T>C NP_001277006.1:p.Tyr277=
NM_001290078.1:c.519T>C NP_001277007.1:p.Tyr173=
XM_005251561.1:c.831T>C XP_005251618.1:p.Tyr277=
XM_005251563.1:c.831T>C XP_005251620.1:p.Tyr277=
XM_005251561.2:c.831T>C XP_005251618.1:p.Tyr277=
XM_005251563.2:c.831T>C XP_005251620.1:p.Tyr277=
NM_000459.5:c.831T>C MANE Select NP_000450.3:p.Tyr277=
NM_001375475.1:c.831T>C NP_001362404.1:p.Tyr277=
NM_001375476.1:c.831T>C NP_001362405.1:p.Tyr277=