Revel Score:
ENST00000262948 (MANE Select)
0.782
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4117561A>C , CM000681.2:g.4117561A>C | GRCh38 |
| NC_000019.9:g.4117559A>C , CM000681.1:g.4117559A>C | GRCh37 |
| NC_000019.8:g.4068559A>C | NCBI36 |
| NG_007996.1:g.11568T>G , LRG_750:g.11568T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394867.9:n.600T>G | ||
| ENST00000687128.1:n.600T>G | ||
| ENST00000262948.10:c.161T>G MANE Select | ENSP00000262948.4:p.Leu54Arg | |
| ENST00000262948.9:c.161T>G | ENSP00000262948.3:p.Leu54Arg | |
| ENST00000394867.8:c.-131T>G | ENSP00000378336.1:n.-131T>G | |
| ENST00000599345.1:n.358T>G | ||
| NM_030662.3:c.161T>G , LRG_750t1:c.161T>G | NP_109587.1:p.Leu54Arg | |
| XM_006722799.2:c.161T>G | XP_006722862.1:p.Leu54Arg | |
| XM_017026989.1:c.161T>G | XP_016882478.1:p.Leu54Arg | |
| XM_017026990.1:c.161T>G | XP_016882479.1:p.Leu54Arg | |
| XM_017026991.1:c.161T>G | XP_016882480.1:p.Leu54Arg | |
| NM_030662.4:c.161T>G MANE Select | NP_109587.1:p.Leu54Arg |