Revel Score:
ENST00000225964 (MANE Select)
0.724
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50186871C>A , CM000679.2:g.50186871C>A | GRCh38 |
| NC_000017.10:g.48264232C>A , CM000679.1:g.48264232C>A | GRCh37 |
| NC_000017.9:g.45619231C>A | NCBI36 |
| NG_007400.1:g.19769G>T , LRG_1:g.19769G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225964.10:c.3583G>T MANE Select | ENSP00000225964.6:p.Gly1195Cys | |
| ENST00000225964.9:c.3583G>T | ENSP00000225964.5:p.Gly1195Cys | |
| ENST00000510710.3:n.252G>T | ||
| NM_000088.3:c.3583G>T , LRG_1t1:c.3583G>T | NP_000079.2:p.Gly1195Cys | |
| XM_005257058.3:c.3313G>T | XP_005257115.2:p.Gly1105Cys | |
| XM_005257059.3:c.2665G>T | XP_005257116.2:p.Gly889Cys | |
| XM_011524341.1:c.3385G>T | XP_011522643.1:p.Gly1129Cys | |
| XM_005257058.4:c.3313G>T | XP_005257115.2:p.Gly1105Cys | |
| XM_005257059.4:c.2665G>T | XP_005257116.2:p.Gly889Cys | |
| NM_000088.4:c.3583G>T MANE Select | NP_000079.2:p.Gly1195Cys |