MyVariant.info:
GRCh37
chr5:g.176522416C>T
Revel Score:
ENST00000511076
0.142
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.177095415C>T , CM000667.2:g.177095415C>T | GRCh38 |
| NC_000005.9:g.176522416C>T , CM000667.1:g.176522416C>T | GRCh37 |
| NC_000005.8:g.176455022C>T | NCBI36 |
| NG_012067.1:g.13496C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000292408.9:c.1605C>T MANE Select | ENSP00000292408.4:p.Asn535= | |
| ENST00000292408.8:c.1605C>T | ENSP00000292408.4:p.Asn535= | |
| ENST00000393637.5:c.1485C>T | ENSP00000377254.1:p.Asn495= | |
| ENST00000393648.6:c.1401C>T | ENSP00000377259.2:p.Asn467= | |
| ENST00000483872.2:n.591C>T | ||
| ENST00000502906.5:c.1605C>T | ENSP00000424960.1:p.Asn535= | |
| ENST00000511076.1:c.499C>T | ||
| NM_001291980.1:c.1401C>T | NP_001278909.1:p.Asn467= | |
| NM_002011.4:c.1605C>T | NP_002002.3:p.Asn535= | |
| NM_022963.3:c.1485C>T | NP_075252.2:p.Asn495= | |
| NM_213647.2:c.1605C>T | NP_998812.1:p.Asn535= | |
| XM_005265838.2:c.1605C>T | XP_005265895.1:p.Asn535= | |
| XM_011534464.1:c.1698C>T | XP_011532766.1:p.Asn566= | |
| XM_011534465.1:c.1287C>T | XP_011532767.1:p.Asn429= | |
| XR_941090.1:n.1600C>T | ||
| NM_001354984.1:c.1605C>T | NP_001341913.1:p.Asn535= | |
| NM_213647.3:c.1605C>T MANE Select | NP_998812.1:p.Asn535= | |
| NM_001291980.2:c.1401C>T | NP_001278909.1:p.Asn467= | |
| NM_001354984.2:c.1605C>T | NP_001341913.1:p.Asn535= | |
| NM_002011.5:c.1605C>T | NP_002002.3:p.Asn535= |