This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Revel Score:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37045503C>T , CM000667.2:g.37045503C>T | GRCh38 |
| NC_000005.9:g.37045605C>T , CM000667.1:g.37045605C>T | GRCh37 |
| NC_000005.8:g.37081362C>T | NCBI36 |
| NG_006987.1:g.173621C>T | |
| NG_006987.2:g.173621C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282516.13:c.6404C>T MANE Select | ENSP00000282516.8:p.Thr2135Ile | |
| ENST00000652901.1:c.6404C>T | ENSP00000499536.1:p.Thr2135Ile | |
| ENST00000282516.12:c.6404C>T | ENSP00000282516.8:p.Thr2135Ile | |
| ENST00000448238.2:c.6404C>T | ENSP00000406266.2:p.Thr2135Ile | |
| ENST00000621733.1:c.1-19075C>T | ENSP00000480694.1:n.1-19075C>T | |
| NM_015384.4:c.6404C>T | NP_056199.2:p.Thr2135Ile | |
| NM_133433.3:c.6404C>T | NP_597677.2:p.Thr2135Ile | |
| XM_005248280.2:c.6404C>T | XP_005248337.1:p.Thr2135Ile | |
| XM_005248282.3:c.5660C>T | XP_005248339.2:p.Thr1887Ile | |
| XM_006714467.2:c.6404C>T | XP_006714530.1:p.Thr2135Ile | |
| XM_006714468.1:c.6206C>T | XP_006714531.1:p.Thr2069Ile | |
| XM_011514014.1:c.6023C>T | XP_011512316.1:p.Thr2008Ile | |
| XM_011514015.1:c.6404C>T | XP_011512317.1:p.Thr2135Ile | |
| XM_005248280.3:c.6404C>T | XP_005248337.1:p.Thr2135Ile | |
| XM_005248282.5:c.5744C>T | XP_005248339.3:p.Thr1915Ile | |
| XM_006714468.2:c.6206C>T | XP_006714531.1:p.Thr2069Ile | |
| XM_017009329.1:c.6404C>T | XP_016864818.1:p.Thr2135Ile | |
| XM_017009330.2:c.4787C>T | XP_016864819.1:p.Thr1596Ile | |
| XM_017009331.1:c.4778C>T | XP_016864820.1:p.Thr1593Ile | |
| NM_133433.4:c.6404C>T MANE Select | NP_597677.2:p.Thr2135Ile | |
| NM_015384.5:c.6404C>T | NP_056199.2:p.Thr2135Ile |