Linked Data
MyVariant Identifiers:
chr11:g.121008179A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121137470A>G , CM000673.2:g.121137470A>G | GRCh38 |
| NC_000011.9:g.121008179A>G , CM000673.1:g.121008179A>G | GRCh37 |
| NC_000011.8:g.120513389A>G | NCBI36 |
| NG_011633.1:g.39805A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392793.6:c.2991A>G (TECTA) MANE Select | ENSP00000376543.1:p.Thr997= | |
| ENST00000642222.1:c.2991A>G (TECTA) | ENSP00000493855.1:p.Thr997= | |
| ENST00000645008.1:c.298A>G (TECTA) | ||
| ENST00000264037.2:c.2991A>G (TECTA) | ENSP00000264037.2:p.Thr997= | |
| ENST00000392793.5:c.2991A>G (TECTA) | ENSP00000376543.1:p.Thr997= | |
| NM_005422.2:c.2991A>G (TECTA) | NP_005413.2:p.Thr997= | |
| NM_001378761.1:c.3948A>G (TBCEL-TECTA) | NP_001365690.1:p.Thr1316= | |
| NM_005422.4:c.2991A>G (TECTA) MANE Select | NP_005413.2:p.Thr997= |