Linked Data
ClinVar Variation Id:
1120105
ClinVar RCV Id:
RCV001449773
dbSNP Id:
rs1408773314
gnomAD v4:
11-121137474-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121137474A>G , CM000673.2:g.121137474A>G | GRCh38 |
| NC_000011.9:g.121008183A>G , CM000673.1:g.121008183A>G | GRCh37 |
| NC_000011.8:g.120513393A>G | NCBI36 |
| NG_011633.1:g.39809A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392793.6:c.2995A>G (TECTA) MANE Select | ENSP00000376543.1:p.Thr999Ala | |
| ENST00000642222.1:c.2995A>G (TECTA) | ENSP00000493855.1:p.Thr999Ala | |
| ENST00000645008.1:c.302A>G (TECTA) | ||
| ENST00000264037.2:c.2995A>G (TECTA) | ENSP00000264037.2:p.Thr999Ala | |
| ENST00000392793.5:c.2995A>G (TECTA) | ENSP00000376543.1:p.Thr999Ala | |
| NM_005422.2:c.2995A>G (TECTA) | NP_005413.2:p.Thr999Ala | |
| NM_001378761.1:c.3952A>G (TBCEL-TECTA) | NP_001365690.1:p.Thr1318Ala | |
| NM_005422.4:c.2995A>G (TECTA) MANE Select | NP_005413.2:p.Thr999Ala |