Revel Score:
ENST00000339994 (MANE Select)
0.299
ENST00000528731
0.299
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17387262T>A , CM000673.2:g.17387262T>A | GRCh38 |
| NC_000011.9:g.17408809T>A , CM000673.1:g.17408809T>A | GRCh37 |
| NC_000011.8:g.17365385T>A | NCBI36 |
| NG_012446.1:g.6398A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682350.1:c.569A>T | ENSP00000508090.1:p.His190Leu | |
| ENST00000682764.1:c.569A>T | ENSP00000506780.1:p.His190Leu | |
| ENST00000339994.5:c.830A>T MANE Select | ENSP00000345708.4:p.His277Leu | |
| ENST00000339994.4:c.830A>T | ENSP00000345708.4:p.His277Leu | |
| ENST00000528731.1:c.569A>T | ENSP00000434755.1:p.His190Leu | |
| NM_000525.3:c.830A>T | NP_000516.3:p.His277Leu | |
| NM_001166290.1:c.569A>T | NP_001159762.1:p.His190Leu | |
| XM_006718226.2:c.569A>T | XP_006718289.1:p.His190Leu | |
| XR_930867.1:n.988A>T | ||
| XM_006718226.3:c.569A>T | XP_006718289.1:p.His190Leu | |
| XM_017017680.1:c.569A>T | XP_016873169.1:p.His190Leu | |
| NM_001166290.2:c.569A>T | NP_001159762.1:p.His190Leu | |
| NM_001377296.1:c.569A>T | NP_001364225.1:p.His190Leu | |
| NM_001377297.1:c.569A>T | NP_001364226.1:p.His190Leu | |
| NM_000525.4:c.830A>T MANE Select | NP_000516.3:p.His277Leu |