Revel Score:
ENST00000318410 (MANE Select)
0.486
ENST00000517845
0.486
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.125061192T>C , CM000670.2:g.125061192T>C | GRCh38 |
| NC_000008.10:g.126073434T>C , CM000670.1:g.126073434T>C | GRCh37 |
| NC_000008.9:g.126142616T>C | NCBI36 |
| NG_012636.1:g.35628A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318410.12:c.1411A>G MANE Select | ENSP00000318016.7:p.Asn471Asp | |
| ENST00000318410.11:c.1411A>G | ENSP00000318016.7:p.Asn471Asp | |
| ENST00000517845.5:c.967A>G | ENSP00000429676.1:p.Asn323Asp | |
| NM_014846.3:c.1411A>G | NP_055661.3:p.Asn471Asp | |
| XM_005251120.2:c.967A>G | XP_005251177.1:p.Asn323Asp | |
| XM_011517409.1:c.1411A>G | XP_011515711.1:p.Asn471Asp | |
| XM_011517410.1:c.1411A>G | XP_011515712.1:p.Asn471Asp | |
| NM_001330609.1:c.967A>G | NP_001317538.1:p.Asn323Asp | |
| XM_017014113.2:c.1411A>G | XP_016869602.1:p.Asn471Asp | |
| NM_014846.4:c.1411A>G MANE Select | NP_055661.3:p.Asn471Asp | |
| NM_001330609.2:c.967A>G | NP_001317538.1:p.Asn323Asp |