Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52029695T= , CM000666.2:g.52029695T= | GRCh38 |
| NC_000004.11:g.52895861T= , CM000666.1:g.52895861T= | GRCh37 |
| NC_000004.10:g.52590618T= | NCBI36 |
| NG_008891.1:g.13625A= , LRG_204:g.13625A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.412A= MANE Select | ENSP00000370839.6:p.Thr138= | |
| ENST00000381431.9:c.412A= | ENSP00000370839.5:p.Thr138= | |
| ENST00000506357.5:c.495A= | ||
| ENST00000514133.1:c.489A= | ENSP00000425818.1:n.489A= | |
| NM_000232.4:c.412A= , LRG_204t1:c.412A= | NP_000223.1:p.Thr138= | |
| XM_006714049.2:c.115A= | XP_006714112.1:p.Thr39= | |
| XM_011534403.1:c.202A= | XP_011532705.1:p.Thr68= | |
| XM_011534404.1:c.115A= | XP_011532706.1:p.Thr39= | |
| NM_000232.5:c.412A= MANE Select | NP_000223.1:p.Thr138= |