Revel Score:
ENST00000418964
0.307
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160706543G>C , CM000668.2:g.160706543G>C | GRCh38 |
| NC_000006.11:g.161127575G>C , CM000668.1:g.161127575G>C | GRCh37 |
| NC_000006.10:g.161047565G>C | NCBI36 |
| NG_016200.1:g.9351G>C , LRG_571:g.9351G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297289.9:c.49+4190G>C | ENSP00000516619.1:n.49+4190G>C | |
| ENST00000418964.2:c.186G>C | ENSP00000389424.2:p.Arg62Ser | |
| ENST00000494325.2:c.-41+1G>C | ENSP00000516620.1:n.-41+1G>C | |
| ENST00000706906.1:c.185+1G>C | ENSP00000516618.1:n.185+1G>C | |
| ENST00000308192.14:c.185+1G>C MANE Select | ENSP00000308938.9:n.185+1G>C | |
| ENST00000297289.8:n.94+4190G>C | ||
| ENST00000308192.13:c.185+1G>C | ENSP00000308938.9:n.185+1G>C | |
| ENST00000366924.6:c.185+1G>C | ENSP00000355891.2:n.185+1G>C | |
| ENST00000418964.1:c.186G>C | ENSP00000389424.1:p.Arg62Ser | |
| ENST00000462918.5:n.222+1G>C | ||
| ENST00000471691.1:n.168+1G>C | ||
| ENST00000483038.5:n.198+1G>C | ||
| ENST00000484367.5:n.1155+1G>C | ||
| ENST00000494325.1:n.169+1G>C | ||
| NM_000301.3:c.185+1G>C , LRG_571t1:c.185+1G>C | NP_000292.1:n.185+1G>C | |
| NM_001168338.1:c.185+1G>C , LRG_571t2:c.185+1G>C | NP_001161810.1:n.185+1G>C | |
| NM_000301.4:c.185+1G>C | NP_000292.1:n.185+1G>C | |
| NM_000301.5:c.185+1G>C MANE Select | NP_000292.1:n.185+1G>C |