Revel Score:
ENST00000261590 (MANE Select)
0.173
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31522128A>T , CM000680.2:g.31522128A>T | GRCh38 |
| NC_000018.9:g.29102091A>T , CM000680.1:g.29102091A>T | GRCh37 |
| NC_000018.8:g.27356089A>T | NCBI36 |
| NG_007072.3:g.28887A>T , LRG_397:g.28887A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682087.2:n.400A>T | ||
| ENST00000682241.2:c.569A>T | ENSP00000507600.2:p.Asn190Ile | |
| ENST00000683614.2:n.400A>T | ||
| ENST00000682087.1:c.400A>T | ||
| ENST00000682241.1:c.400A>T | ||
| ENST00000683614.1:c.400A>T | ||
| ENST00000683654.1:c.569A>T | ENSP00000506971.1:p.Asn190Ile | |
| ENST00000684461.1:n.1239A>T | ||
| ENST00000261590.13:c.569A>T MANE Select | ENSP00000261590.8:p.Asn190Ile | |
| ENST00000261590.12:c.569A>T | ENSP00000261590.8:p.Asn190Ile | |
| ENST00000585206.1:c.569A>T | ENSP00000462503.1:p.Asn190Ile | |
| NM_001943.3:c.569A>T , LRG_397t1:c.569A>T | NP_001934.2:p.Asn190Ile | |
| NM_001943.4:c.569A>T | NP_001934.2:p.Asn190Ile | |
| XM_024451095.1:c.35A>T | XP_024306863.1:p.Asn12Ile | |
| NM_001943.5:c.569A>T MANE Select | NP_001934.2:p.Asn190Ile |