Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121130157G= , CM000673.2:g.121130157G= | GRCh38 |
| NC_000011.9:g.121000866G= , CM000673.1:g.121000866G= | GRCh37 |
| NC_000011.8:g.120506076G= | NCBI36 |
| NG_011633.1:g.32492G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005422.4:c.2887G= (TECTA) MANE Select | NP_005413.2:p.Ala963= |
| ENST00000392793.6:c.2887G= (TECTA) MANE Select | ENSP00000376543.1:p.Ala963= |
| NM_001378761.1:c.3844G= (TBCEL-TECTA) | NP_001365690.1:p.Ala1282= |
| NM_005422.2:c.2887G= (TECTA) | NP_005413.2:p.Ala963= |
| ENST00000264037.2:c.2887G= (TECTA) | ENSP00000264037.2:p.Ala963= |
| ENST00000392793.5:c.2887G= (TECTA) | ENSP00000376543.1:p.Ala963= |
| ENST00000642222.1:c.2887G= (TECTA) | ENSP00000493855.1:p.Ala963= |
| ENST00000645008.1:c.194G= (TECTA) |