Revel Score:
ENST00000265104 (MANE Select)
0.645
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00001376 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Exomes Max Group AF
0.00001295 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13840968G>C , CM000667.2:g.13840968G>C | GRCh38 |
| NC_000005.9:g.13841077G>C , CM000667.1:g.13841077G>C | GRCh37 |
| NC_000005.8:g.13894077G>C | NCBI36 |
| NG_013081.1:g.108513C>G | |
| NG_013081.2:g.108513C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.5647C>G MANE Select | ENSP00000265104.4:p.Arg1883Gly | |
| ENST00000681290.1:c.5602C>G | ENSP00000505288.1:p.Arg1868Gly | |
| ENST00000265104.4:c.5647C>G | ENSP00000265104.4:p.Arg1883Gly | |
| NM_001369.2:c.5647C>G | NP_001360.1:p.Arg1883Gly | |
| XM_005248262.2:c.5602C>G | XP_005248319.1:p.Arg1868Gly | |
| XM_011513990.1:c.5647C>G | XP_011512292.1:p.Arg1883Gly | |
| XR_925598.1:n.5854C>G | ||
| XM_005248262.3:c.5755C>G | XP_005248319.2:p.Arg1919Gly | |
| XM_017009177.1:c.5755C>G | XP_016864666.1:p.Arg1919Gly | |
| XM_017009178.1:c.4660C>G | XP_016864667.1:p.Arg1554Gly | |
| XM_017009179.2:c.4660C>G | XP_016864668.1:p.Arg1554Gly | |
| XM_017009180.1:c.5755C>G | XP_016864669.1:p.Arg1919Gly | |
| XM_017009181.1:c.5755C>G | XP_016864670.1:p.Arg1919Gly | |
| XM_017009182.1:c.5755C>G | XP_016864671.1:p.Arg1919Gly | |
| XM_017009183.1:c.5755C>G | XP_016864672.1:p.Arg1919Gly | |
| XM_017009184.1:c.5755C>G | XP_016864673.1:p.Arg1919Gly | |
| XM_017009185.1:c.844C>G | XP_016864674.1:p.Arg282Gly | |
| XM_017009186.1:c.397C>G | XP_016864675.1:p.Arg133Gly | |
| XM_017009187.1:c.5755C>G | XP_016864676.1:p.Arg1919Gly | |
| XM_024454388.1:c.4660C>G | XP_024310156.1:p.Arg1554Gly | |
| XM_024454389.1:c.4249C>G | XP_024310157.1:p.Arg1417Gly | |
| XR_001742034.1:n.5772C>G | ||
| XR_001742035.1:n.5772C>G | ||
| NM_001369.3:c.5647C>G MANE Select | NP_001360.1:p.Arg1883Gly |